PropertyValue
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.w3.org/ns/prov#value
  • The individual will also be responsible for authoring and/or review of Safety Pharmacology and Toxicology sections of all regulatory documents, including IND, CTA, IB, annual reports, and NDA/MAA submissions.
http://www.w3.org/ns/prov#wasQuotedFrom
  • startuphire.com