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- NCIT_C165826 IAO_0000115 "Medicinal products given to the subject as an aid to assess a relevant clinical trial end-point; it is not being tested or used as a reference in the clinical trial. (Recommendations from the expert group on clinical trials for the implementation of Regulation (EU) No 536/2014' dd 28 June 2017)" @default.
- NCIT_C165826 NCIT_NHC0 "C165826" @default.
- NCIT_C165826 NCIT_P106 "Chemical Viewed Functionally" @default.
- NCIT_C165826 NCIT_P108 "End-point Assessment Medicinal Product" @default.
- NCIT_C165826 NCIT_P208 "CL979056" @default.
- NCIT_C165826 NCIT_P322 "CDISC-GLOSS" @default.
- NCIT_C165826 NCIT_P325 "Medicinal products given to the subject as an aid to assess a relevant clinical trial end-point; it is not being tested or used as a reference in the clinical trial. [After Recommendations from the expert group on clinical trials for the implementation of Regulation (EU) No 536/2014' dd 28 June 2017]" @default.
- NCIT_C165826 normalizedInformationContent "100" @default.
- NCIT_C165826 referenceCount "1" @default.
- NCIT_C165826 hasExactSynonym "End-point Assessment Medicinal Product" @default.
- NCIT_C165826 hasExactSynonym "end-point assessment medicinal product" @default.
- NCIT_C165826 inSubset NCIT_C61410 @default.
- NCIT_C165826 inSubset NCIT_C67497 @default.
- NCIT_C165826 type Class @default.
- NCIT_C165826 isDefinedBy ncit.owl @default.
- NCIT_C165826 label "End-point Assessment Medicinal Product" @default.
- NCIT_C165826 subClassOf NCIT_C142605 @default.
- NCIT_C165826 subClassOf NCIT_C156473 @default.
- NCIT_C165826 subClassOf NCIT_C165826 @default.
- NCIT_C165826 subClassOf NCIT_C1708 @default.
- NCIT_C165826 subClassOf NCIT_C20181 @default.