PropertyValue
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.w3.org/ns/prov#value
  • clinical trials, together with preclinical data and other supporting information that establishes a drug candidate??s safety, are submitted to the FDA in the form of a NDA or NDA supplement (for approval of a new indication if the product
http://www.w3.org/ns/prov#wasQuotedFrom
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