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- NCIT_C54698 IAO_0000115 "The examination of data and information in an application for premarket review described in sections 505, 510(k), 513(f), 515, or 520(g) or 520(l) of the Federal Food, Drug, and Cosmetic Act or section 351 of the Public Health Service Act of data and information contained in any investigational new drug application, investigational device exemption, new drug application, biologics license application, device premarket notification, device reclassification petition, and premarket approval application." @default.
- NCIT_C54698 NCIT_NHC0 "C54698" @default.
- NCIT_C54698 NCIT_P106 "Activity" @default.
- NCIT_C54698 NCIT_P108 "Premarket Review" @default.
- NCIT_C54698 NCIT_P207 "C1882447" @default.
- NCIT_C54698 NCIT_P366 "Premarket_Review" @default.
- NCIT_C54698 normalizedInformationContent "100" @default.
- NCIT_C54698 referenceCount "1" @default.
- NCIT_C54698 hasExactSynonym "Premarket Review" @default.
- NCIT_C54698 type Class @default.
- NCIT_C54698 isDefinedBy ncit.owl @default.
- NCIT_C54698 label "Premarket Review" @default.
- NCIT_C54698 subClassOf NCIT_C25404 @default.
- NCIT_C54698 subClassOf NCIT_C42729 @default.
- NCIT_C54698 subClassOf NCIT_C43431 @default.
- NCIT_C54698 subClassOf NCIT_C54697 @default.
- NCIT_C54698 subClassOf NCIT_C54698 @default.