About: http://webisa.webdatacommons.org/2423368

Property	Value
http://www.w3.org/1999/02/22-rdf-syntax-ns#type	http://www.w3.org/ns/prov#Entity
http://www.w3.org/ns/prov#value	Moreover, very recent work has shown that specific Shp2 mutations are the cause of certain rare forms of leukemia as well as the most common human autosomal dominant genetic disease, Noonan syndrome.
http://www.w3.org/ns/prov#wasQuotedFrom	cancer.gov