Head noun: mutation

Same concepts
http://dbpedia.org/resource/Mutation

Broader concepts

labelprovenanceconfidence
genetic alterationisap:1821272550.775863
natural processisap:3471562670.691929
eventisap:3620448910.673951
genetic abnormalityisap:832342720.616304
fundamental life processisap:3471562730.605311
ga operatorisap:605659710.590179
unconscious mechanismisap:1827956150.577629
biological processisap:3471562700.561481
genotypic changeisap:4806850820.553867
genetic mechanismisap:1827956100.547006
change in the dnaisap:4806850510.544597
genomic aberrationisap:1806581340.515859
specific genetic alterationisap:1821272680.514058
genetic damageisap:4805059980.511266
significant biological effectisap:4861837290.509065
alterationisap:1821272540.504279
germline mutationisap:630150810.497368
genetic problemisap:3472066030.493760
meansisap:3573603490.488266
deleterious mutationisap:630151530.486355
basic genetic operatorisap:605659760.478487
random processisap:3471562660.475556
random eventisap:3620448920.474491
source of genetic variationisap:4822657500.470777
thingisap:3641123490.470720
factorisap:4821225340.468577
genetic changeisap:4806850490.462470
serious biological consequenceisap:832592570.462021
alteration in cancer cellisap:1821272590.459733
dramatic changeisap:4806850870.454753
external factorisap:4821225860.447844
random forceisap:3611200580.441645
nucleotide sequenceisap:579998180.441584
variationisap:1861771120.441519
genetic variationisap:1861771130.439170
various mechanismisap:1827956210.438964
natural selectionisap:1834511620.438268
genetic anomalyisap:3416290960.432077
operationisap:1832104840.431420
gene variationisap:1861771150.430749
evolutionary eventisap:3620449080.430178
stochastic eventisap:3620449010.429572
disease-causing mutationisap:630151310.427338
multiple mechanismisap:1827956260.426718
influenza a virusisap:3606066100.426010
genetic operationisap:1832104850.423849
cause of hereditary hemochromatosisisap:3641633800.421316
mechanism of genetic variationisap:1827956250.419866
land recordsisap:3445369090.418470
conceptisap:3438628640.418255
genetic mutationisap:630150880.418226
change in the sequenceisap:4806850520.417495
evolutionary mechanismisap:1827956090.415833
evolutionary historyisap:3429856330.413134
recurrent mutationisap:630151650.411706
genetic factorisap:4821225410.411489
change in a geneisap:4806850500.406146
evolutionary principleisap:1851890120.405723
change in a cell'isap:4806851020.403729
mechanism of evolutionary changeisap:1827956330.403278
source of variationisap:4822657480.402079
sequence alterationisap:1821272780.401493
point mutationisap:630150710.400843
evolutionary changeisap:4806850960.399208
change in geneisap:4806850770.397125
p53 functionisap:569063120.396978
specific nucleic acid sequenceisap:579998110.393833
rare variantisap:3463094200.393674
mismatchisap:632045890.393668
amino acid substitutionisap:3222147320.391372
errorisap:3623596580.391179
changeisap:4806850480.389796
genomic instabilityisap:827757160.388710
specific mutationisap:630150870.385033
health problemisap:3472066050.380737
different mutationisap:630150840.377525
recessive mutationisap:630150850.375165
nonsense mutationisap:630150790.374159
defectisap:4782253170.373446
perturbationisap:3219760190.369248
good ideaisap:3824361960.368292
stochastic processisap:3471562740.363996
novel mutationisap:630150890.363792
side effectisap:4861837280.362763
common mutationisap:630151370.362059
dna changeisap:4806850630.358028
alteration in the dnaisap:1821272610.349594
evolutionary processisap:3471562680.348546
formisap:3825777900.344318
undirected processisap:3471562830.340283
driver mutationisap:630150940.339573
variantisap:3463094140.333700
many factorisap:4821225800.330676
change in dnaisap:4806850560.329604
survival advantageisap:1839421040.327602
random errorisap:3623596600.326201
explanationisap:844499780.325480
blind processisap:3471562780.325390
dna damageisap:4805060000.324970
genetic materialisap:585917860.324895
mechanism of evolutionisap:1827956290.324458
genetic operatorisap:605659690.323120
health riskisap:3811276220.321877
rare eventisap:3620448980.318685
ion channelisap:3434236080.318196
biological mechanismisap:1827956120.317401
issueisap:3593951770.317065
protein expressionisap:1817955110.312154
gene duplicationisap:836751670.310054
random operationisap:1832104880.309566
missense mutationisap:630150780.308081
coding sequenceisap:579998090.308065
abnormalityisap:832342710.307250
independent eventisap:3620449030.305542
single substitutionisap:3222147380.303700
complex diseaseisap:3451984700.299658
darwinian meansisap:3573603500.297799
snpisap:3486293270.295997
recessive traitisap:3610487330.293752
chromosomal aberrationisap:1806581350.293286
recessive geneisap:3825553150.291817
amino acid changeisap:4806850940.288672
many reasonisap:4846804090.288382
random mechanismisap:1827956170.285792
geneticsisap:600559410.285504
base pair deletionisap:608539400.280795
processisap:3471562650.278908
change in genetic informationisap:4806850890.277283
modificationisap:3217591760.274866
frameshift mutationisap:630151670.271559
conditionisap:1855295780.262532
psychiatric disorderisap:622273290.262280
parameterisap:1857890710.259520
polymorphismisap:3222740690.253438
percent chanceisap:4806872000.252820
characteristicisap:637216180.251505
reasonisap:4846804080.249012
beneficial mutationisap:630151030.246850
accidentisap:584819740.245908
genetic profileisap:3472705230.245305
different mechanismisap:1827956190.244493
new game modeisap:3826942500.243892
genetic informationisap:829223860.242564
genome instabilityisap:827757180.242233
cis-regulatory mutationisap:630151380.237697
nucleic acidisap:3823880660.235233
cellular damageisap:4805060010.234278
deletion mutationisap:630150910.232885
other factorisap:4821225450.232633
molecular diagnosticisap:1823160880.232633
expansionisap:1838618020.231844
methodisap:4813695050.231606
abilityisap:3411957970.231190
typeisap:3812828380.230708
amino acid sequenceisap:579998070.229872
chromosomal rearrangementisap:1526374180.226784
lesionisap:4860014270.226566
skill in the artisap:3628697830.226382
manipulationisap:3223284040.225991
evolutionisap:1833824120.225782
nucleotide changeisap:4806850610.224700
risk factorisap:4821225420.224122
band unlike any otherisap:3823272830.220690
developmentisap:841572710.220483
effectisap:4861837240.220383
complexityisap:1802474520.219030
natural variantisap:3463094240.218764
forceisap:3611200550.218362
probabilityisap:837800970.217578
mechanismisap:1827956060.213565
lifespanisap:573329400.212815
sequenceisap:579998030.212110
knowledgeisap:1841210980.211485
target geneisap:3825553300.211231
partisap:3812485680.211062
c elegansisap:3449989120.210860
versionisap:3468035460.209504
genomic featureisap:3418060250.209179
catastropheisap:837662970.209062
breast cancerisap:4849470400.208556
common oneisap:3486239240.208361
findingisap:3423876240.208049
questionisap:624950610.207999
major sourceisap:4822657490.207884
organismisap:614533710.206666
large deletionisap:608539330.203620
phenomenonisap:1822501400.202987
recordisap:4850970200.202723
featureisap:3418060240.202538
threatisap:4839564280.202414
wordisap:3816300950.201735
operatorisap:605659700.200987
offspringisap:1865546760.199254
healthisap:4782277610.198256
strategyisap:608434230.197464
actionisap:4850453180.196935
disruptionisap:1806550580.196840
oneisap:3486239200.196415
simulation of evolutionisap:1822561340.196382
outputisap:4833200410.196254
riskisap:3811276150.191161
problemisap:3472066010.190723
strainisap:4800761390.190210
animalisap:4847475030.189795
optimizationisap:3220820550.189007
populationisap:1815088310.188324
respectivelyisap:3220354740.188266
deletionisap:608539300.187617
event in the developmentisap:3620448950.187460
aisap:632685680.186873
small deletionisap:608539340.185452
compoundisap:592703070.184834
evolutionary theoryisap:4836415990.183085
principleisap:1851890110.182985
example of evolutionisap:3436271630.182434
genetic disorderisap:622273230.180772
sourceisap:4822657460.180660
transversionisap:3216063910.179465
antibiotic resistanceisap:1817643190.177231
intelligenceisap:3223257810.176675
present inventionisap:1863106380.176314
cancerisap:4849470060.174906
simulationisap:1822561330.174850
common causeisap:3641633010.174460
cancer cellisap:3822766800.173179
loss of informationisap:3827493740.172375
embodiment of the inventionisap:1800933550.172288
part of the processisap:3812485690.170032
inisap:4078256580.169920
part of lifeisap:3812485730.169091
sameisap:3814327330.168964
nonsenseisap:614400260.168934
insertionisap:1862883100.168921
componentisap:1857950260.168072
inheritanceisap:840593630.166851
survivalisap:601788980.165798
stressisap:4800832590.164898
part of evolutionisap:3812485710.164727
moreoverisap:613606530.163117
elementisap:3426707320.162346
chromosomeisap:1809207280.161786
pointisap:3623561230.161400
damageisap:4805059990.160519
deletion in exon 19isap:608539360.160237
possibilityisap:836022430.159808
enzymeisap:4818277540.159709
additionisap:617089650.159407
respectisap:3467743940.158544
exampleisap:3436271620.157077
good pointisap:3623561240.156815
brain powerisap:3623375620.155926
adaptationisap:1814792240.155039
behaviorisap:594029710.154905
causeisap:3641632790.154814
godisap:3486124070.154680
brafisap:3823543660.154607
informationisap:829223850.153146
aberrationisap:1806581370.150695
indicatorisap:1862755820.150547
type collagenisap:579726120.150016
disadvantageisap:3218233090.149898
numberisap:4848046790.149647
double-edged swordisap:3635629040.148931
chanceisap:4806871980.148054
responseisap:578128650.147599
discoveryisap:1853105360.146092
givenisap:3632892630.145936
wellisap:3816683190.143628
deformityisap:1850862120.143162
anythingisap:579035700.141553
otherisap:3638403050.141322
cohortisap:4858130150.141010
pmisap:4078136870.140873
researcherisap:1805862650.140770
bodyisap:3823172400.140208
stem cellisap:3822766790.140014
good exampleisap:3436271660.139905
molecular biologyisap:3429605950.139301
oddsisap:3811874800.139279
gisap:632685220.138462
observationisap:835913320.138319
investigatorisap:3221899990.138027
good thingisap:3641123510.137909
disorderisap:622273180.137677
techniqueisap:1830441150.137392
additionallyisap:3222214410.136758
entire genomeisap:4835433480.136748
bad thingisap:3641123560.136395
mutationisap:630150690.134804
amino acidisap:3823880670.134374
duplicationisap:836751640.134308
splice siteisap:3814151610.133117
patientisap:3439095480.132875
nucleotideisap:1811529020.132371
hallmarkisap:569943240.131893
statementisap:1839884970.130147
mutagenisap:3475307180.129967
seriesisap:4846674890.129796
parentisap:4811211560.129131
adisap:4078247430.129075
polypeptideisap:826496470.128651
improvementisap:830272710.128253
relationshipisap:3219476890.128167
dead endisap:3486167940.128095
mutagenesisisap:827012750.128028
base deletion at codonisap:608539420.127949
optionisap:4836047180.127940
accumulationisap:3215941850.127533
maleisap:3827185380.127367
quantityisap:571486790.127025
inventionisap:1863106390.126765
channelisap:3434236090.126688
identificationisap:637364800.126342
growthisap:4816358400.126329
frameshiftisap:1801666400.126078
presenceisap:587407910.125040
courseisap:4845294920.124102
secondisap:4848453200.123668
mutantisap:4827781560.123650
matterisap:4819930290.123633
varietyisap:3462410600.123572
furthermoreisap:841866860.122944
analysisisap:593019430.120268
diseaseisap:3451984500.119730
functionisap:569063080.118447
combinationisap:841591480.118241
timeisap:3814880910.118155
generationisap:1804339810.118056
termisap:3814938380.117187
factisap:3826189730.116704
wild typeisap:3812828450.115285
cisap:632686290.114149
sequencingisap:1820980370.113579
individualisap:1811321400.113252
toolisap:3814830320.111953
modelisap:3578612310.111937
peopleisap:4805887980.111275
phenotypeisap:1847221700.110456
systemisap:4786172030.110425
proteinisap:3442755130.110310
henceisap:3579731810.110266
randomisap:4863270940.109537
andisap:3486108190.109484
differenceisap:1816911460.109296
advantageisap:1839421050.109015
measureisap:3414571300.107010
reproductionisap:3221824220.106109
diversityisap:1845093590.105089
knockoutisap:578562300.104707
environmentisap:834595060.104247
mistakeisap:3419047850.103903
indicationisap:1806282700.101568
isisap:4078256760.101332
brainisap:3630197660.100967
restisap:3811202740.100599
geneisap:3825553070.100006
influenza virusisap:3606066120.098441
thereforeisap:1840433170.098035
popisap:3486249800.097451
lossisap:3827493760.097010
instanceisap:627788250.096462
recombinationisap:1530428230.096302
screeningisap:1849680020.096137
ieisap:4078256220.095842
needisap:3811467420.095521
lung cancerisap:4849470390.095506
yearisap:3815321160.093659
genetic testingisap:3476698260.093616
decadeisap:4782878610.093452
imisap:4078256520.093007
disap:632685040.092321
creatureisap:577398490.092004
simplest explanationisap:844499790.091961
caseisap:3823506390.091166
markerisap:4817728700.090996
conformationisap:3217435380.090941
cellisap:3822766740.090832
corruptionisap:1823911730.089836
alleleisap:4812201690.089606
existenceisap:1828718640.089568
amlisap:3486107910.088332
letterisap:4859285820.087809
birdisap:3823084130.087197
realityisap:3413674470.086512
approachisap:621633530.086419
genomeisap:4835433500.086231
contributorisap:837145360.085806
leucineisap:3474664460.085795
situationisap:1864593050.085342
birthisap:3625712370.083204
contributionisap:3214728980.083161
breastisap:4850626720.082429
epilepsyisap:602651310.082303
figureisap:4785505760.082200
relationisap:602080650.081033
datumisap:3583419590.079027
consequenceisap:832592550.078750
embodimentisap:1800933540.077718
nothingisap:3447707490.076632
groupisap:3628613080.075206
paperisap:3615465680.074533
previouslyisap:1807208380.072656
specificityisap:830600250.071360
pleiotropyisap:1817858070.071314
let'isap:3827613910.070393
levelisap:3632221020.070195
roleisap:3814021200.070088
other thingisap:3641123530.068703
natureisap:4851048480.068537
speciesisap:3428910240.067067
dogisap:3486182650.067013
resistanceisap:1817643200.066837
lifeisap:3827557960.065665
bacteriumisap:1852384690.064668
potentialisap:1831143500.063079
howeverisap:3459352580.063032
workisap:3816301200.062515
dnaisap:3486183080.062507
siteisap:3814151600.062373
constraintisap:1807493280.062101
hcmisap:3486219440.062003
studyisap:3633234080.061834
virusisap:3606066090.060793
resultisap:4857265940.059768
womanisap:3586585130.059335
interestisap:571305060.059229
plantisap:3620874230.059146
eyeisap:3486165030.057594
insightisap:3444067180.054887
targetisap:4787800830.054884
cgdisap:3486079220.051711
speculationisap:827766070.050860
tumorisap:3613350710.050854
thusisap:3814858770.050704
hivisap:3486222450.050497
drugisap:3821986770.050407
femaleisap:4798532470.047607
fitnessisap:3419172580.047251
theisap:3486301350.046091
scientistisap:1858660210.042453
otherwiseisap:1861044860.041775
mindisap:3827051400.040721
selectionisap:1834511610.034915
regionisap:4853040280.029749
testisap:3814944040.029744
malignancyisap:1816361000.019414

Narrower concepts

labelprovenanceconfidence
nonsense mutationisap:630150720.705427
founder mutationisap:630151340.668232
single nucleotide polymorphismisap:4261199750.660114
frame shift mutationisap:630151070.657969
single nucleotideisap:2825072900.649866
gene rearrangementisap:640182530.634447
howeverisap:521622690.631501
genetic alterationisap:2829747650.603950
chromosomal translocationisap:640952110.602839
truncationisap:2848417910.594143
factor v leidenisap:1025097570.593080
copy number variationisap:4116824980.581410
cancer mutationisap:630151620.578843
white skinisap:4573454080.557222
splice site mutationisap:630151430.550682
brca2isap:2926715910.548204
microsatellite instabilityisap:4625977080.547792
missense mutationisap:630150750.546286
last man on earthisap:3307960890.543471
neurodegenerative disorderisap:569499650.537575
gene duplicationisap:4631264280.536101
base substitutionisap:4266617100.531988
silent mutationisap:630150970.530182
sickle cell anemiaisap:1052133860.521183
k65risap:4546127080.514599
premature stop codonisap:2923879360.514259
extra limbisap:4616106500.507954
deletion mutationisap:630151020.502424
g551d mutationisap:630151040.500502
large deletionisap:621037260.495263
brca mutationisap:630151060.492124
jak2 v617f mutationisap:630151230.491702
sequence alterationisap:2829747680.486460
m184visap:2949950250.477611
chromosomal fusionisap:1036394110.473321
downs syndromeisap:583073070.473054
nucleotide substitutionisap:4266617090.472830
k103nisap:2941085790.472158
stop codonisap:2923879400.472120
fragile xisap:4723815700.467952
braf v600eisap:2940603190.467533
blue eyeisap:3286125240.465715
cancerisap:1010109190.464500
sickle cellisap:4573069180.458687
g551disap:2989052130.455359
small insertionisap:4122212360.455067
dna codingisap:998663750.435522
small populationisap:2834589020.434973
single-base substitutionisap:4266617140.432486
limited toisap:1405883100.429086
natural selectionisap:4103332450.428241
single nucleotide polymorphism snpsisap:4588695480.428069
splice-site mutationisap:630150950.427871
point mutationisap:630150700.425748
single nucleotide polymorphism snpisap:3321571850.423376
albinismisap:605936950.419617
other handisap:4599787780.414151
amino acid changeisap:997364410.406811
white tigerisap:2940376650.404758
nucleotide polymorphism snpisap:3321571890.403038
white faceisap:4565788760.402318
otherisap:2990085200.398219
variantisap:516199050.397503
gene knockoutisap:631568750.397153
gene silencingisap:4120035990.389161
gene mutationisap:630151270.388426
null mutationisap:630151500.388283
red hairisap:4584152540.387095
first timeisap:4613344120.379347
substitutionisap:4266617070.371773
deletionisap:621037190.366890
oneisap:3292806860.364960
spanish fluisap:3313392480.360663
natureisap:1033508890.358083
lighter skinisap:4573454100.356013
inclusion criterionisap:4097400860.351220
individual geneisap:4570125610.348949
skin colorisap:2959312590.344432
additionisap:605554670.342688
duplicationisap:4631264270.342038
diseaseisap:472144180.338797
polyploidyisap:2840027360.337231
repeat expansionisap:4133391820.337171
delta 32isap:2982805480.334331
sickle-cell anemiaisap:1052133920.329754
present inventionisap:4130235190.327710
environmental stressisap:1062931400.325430
evolutionisap:4113175170.325207
codon 12isap:2923879380.323854
animalisap:1043084500.321946
tentacleisap:580499460.319697
polymorphismisap:4261199740.317556
genetic diseaseisap:472144290.314727
frameshift deletionisap:621037400.313834
dnaisap:3303098840.312565
amino acidisap:4553045570.311839
loss of heterozygosityisap:4548665510.307633
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