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- NCIT_C70875 IAO_0000115 "A regulatory plan or strategy submitted to the FDA proposing the approval of a new device for marketing in the U.S. It includes a demonstration of the safety and efficacy of the device." @default.
- NCIT_C70875 NCIT_NHC0 "C70875" @default.
- NCIT_C70875 NCIT_P106 "Intellectual Product" @default.
- NCIT_C70875 NCIT_P108 "Product Development Protocol" @default.
- NCIT_C70875 NCIT_P207 "C2347689" @default.
- NCIT_C70875 NCIT_P322 "FDA" @default.
- NCIT_C70875 NCIT_P366 "Product_Development_Protocol" @default.
- NCIT_C70875 normalizedInformationContent "100" @default.
- NCIT_C70875 referenceCount "1" @default.
- NCIT_C70875 hasExactSynonym "PDP" @default.
- NCIT_C70875 hasExactSynonym "Product Development Protocol" @default.
- NCIT_C70875 inSubset NCIT_C106039 @default.
- NCIT_C70875 type Class @default.
- NCIT_C70875 isDefinedBy ncit.owl @default.
- NCIT_C70875 label "Product Development Protocol" @default.
- NCIT_C70875 subClassOf NCIT_C19498 @default.
- NCIT_C70875 subClassOf NCIT_C20181 @default.
- NCIT_C70875 subClassOf NCIT_C25198 @default.
- NCIT_C70875 subClassOf NCIT_C60755 @default.
- NCIT_C70875 subClassOf NCIT_C70868 @default.
- NCIT_C70875 subClassOf NCIT_C70875 @default.
- NCIT_C70875 subClassOf NCIT_C73110 @default.
- NCIT_C70875 subClassOf NCIT_C97331 @default.