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- NCIT_C82496 IAO_0000115 "An indication or description of whether the adverse event caused the subject to discontinue from the study." @default.
- NCIT_C82496 NCIT_NHC0 "C82496" @default.
- NCIT_C82496 NCIT_P106 "Finding" @default.
- NCIT_C82496 NCIT_P108 "Adverse Event Caused Study Discontinuation" @default.
- NCIT_C82496 NCIT_P207 "C2826233" @default.
- NCIT_C82496 NCIT_P366 "Adverse_Event_Caused_Study_Discontinuation" @default.
- NCIT_C82496 normalizedInformationContent "100" @default.
- NCIT_C82496 referenceCount "1" @default.
- NCIT_C82496 hasExactSynonym "AEDIS" @default.
- NCIT_C82496 hasExactSynonym "Adverse Event Caused Study Discontinuation" @default.
- NCIT_C82496 inSubset NCIT_C83187 @default.
- NCIT_C82496 inSubset NCIT_C83188 @default.
- NCIT_C82496 type Class @default.
- NCIT_C82496 isDefinedBy ncit.owl @default.
- NCIT_C82496 label "Adverse Event Caused Study Discontinuation" @default.
- NCIT_C82496 subClassOf NCIT_C20181 @default.
- NCIT_C82496 subClassOf NCIT_C20200 @default.
- NCIT_C82496 subClassOf NCIT_C49489 @default.
- NCIT_C82496 subClassOf NCIT_C82496 @default.