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- B1434ce5a20f26cb91c482ec7ba159673 NCIT_P378 "NCI" @default.
- B1434ce5a20f26cb91c482ec7ba159673 type Axiom @default.
- B1434ce5a20f26cb91c482ec7ba159673 annotatedProperty IAO_0000115 @default.
- B1434ce5a20f26cb91c482ec7ba159673 annotatedSource NCIT_C53260 @default.
- B1434ce5a20f26cb91c482ec7ba159673 annotatedTarget "A characteristic used to qualify the adverse event as certainly related to the medical intervention. According to WHO causality assessment criteria of suspected adverse reactions it is applicable to a clinical event, including laboratory test abnormality, occurring in a plausible time relationship to medical intervention, and which cannot be explained by concurrent disease or other interventions. The response to withdrawal of the medical product (dechallenge) should be clinically plausible. The event must be definitive pharmacologically or phenomenologically, using a satisfactory rechallenge procedure if necessary." @default.