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- NCIT_C128520 IAO_0000115 "The healthcare provider or setting must report adverse events of interest to the Manufacturer, MedWatch, and/or a REMS Program." @default.
- NCIT_C128520 NCIT_NHC0 "C128520" @default.
- NCIT_C128520 NCIT_P106 "Activity" @default.
- NCIT_C128520 NCIT_P108 "Report Adverse Events" @default.
- NCIT_C128520 NCIT_P208 "CL509312" @default.
- NCIT_C128520 NCIT_P322 "FDA" @default.
- NCIT_C128520 normalizedInformationContent "100" @default.
- NCIT_C128520 referenceCount "1" @default.
- NCIT_C128520 hasExactSynonym "Report Adverse Events" @default.
- NCIT_C128520 inSubset NCIT_C128491 @default.
- NCIT_C128520 inSubset NCIT_C54452 @default.
- NCIT_C128520 type Class @default.
- NCIT_C128520 isDefinedBy ncit.owl @default.
- NCIT_C128520 label "Report Adverse Events" @default.
- NCIT_C128520 subClassOf NCIT_C128494 @default.
- NCIT_C128520 subClassOf NCIT_C128520 @default.
- NCIT_C128520 subClassOf NCIT_C43431 @default.
- NCIT_C128520 subClassOf NCIT_C49235 @default.