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- NCIT_C139173 IAO_0000115 "An auxiliary endpoint associated with the study or trial." @default.
- NCIT_C139173 NCIT_NHC0 "C139173" @default.
- NCIT_C139173 NCIT_P106 "Temporal Concept" @default.
- NCIT_C139173 NCIT_P108 "Secondary Endpoint" @default.
- NCIT_C139173 NCIT_P208 "CL526613" @default.
- NCIT_C139173 NCIT_P322 "CDISC" @default.
- NCIT_C139173 NCIT_P325 "Endpoint(s) that may provide supportive information about the effect of the study intervention(s) on the primary endpoint or demonstrate additional effects on the disease or condition. (After FDA-NIH Protocol Template)" @default.
- NCIT_C139173 normalizedInformationContent "100" @default.
- NCIT_C139173 referenceCount "1" @default.
- NCIT_C139173 hasExactSynonym "Secondary Endpoint" @default.
- NCIT_C139173 inSubset NCIT_C132298 @default.
- NCIT_C139173 inSubset NCIT_C170441 @default.
- NCIT_C139173 inSubset NCIT_C188693 @default.
- NCIT_C139173 inSubset NCIT_C188726 @default.
- NCIT_C139173 inSubset NCIT_C61410 @default.
- NCIT_C139173 type Class @default.
- NCIT_C139173 isDefinedBy ncit.owl @default.
- NCIT_C139173 label "Secondary Endpoint" @default.
- NCIT_C139173 subClassOf NCIT_C139173 @default.
- NCIT_C139173 subClassOf NCIT_C16342 @default.
- NCIT_C139173 subClassOf NCIT_C20047 @default.
- NCIT_C139173 subClassOf NCIT_C25212 @default.