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- NCIT_C76126 IAO_0000115 "An adverse event appears to have occurred, but there does not appear to have been a problem with a medical device or the way it was used." @default.
- NCIT_C76126 NCIT_NHC0 "C76126" @default.
- NCIT_C76126 NCIT_P106 "Qualitative Concept" @default.
- NCIT_C76126 NCIT_P108 "Adverse Event without Identified Device or Use Problem" @default.
- NCIT_C76126 NCIT_P207 "C2698480" @default.
- NCIT_C76126 NCIT_P317 "Device Problem Code (Appendix B)" @default.
- NCIT_C76126 NCIT_P322 "FDA" @default.
- NCIT_C76126 NCIT_P325 "An adverse event (e.g. patient harm) appears to have occurred, but there does not appear to have been a problem with the device or the way it was used." @default.
- NCIT_C76126 NCIT_P366 "No_Known_Device_Problem" @default.
- NCIT_C76126 normalizedInformationContent "100" @default.
- NCIT_C76126 referenceCount "1" @default.
- NCIT_C76126 hasDbXref "IMDRF:A24" @default.
- NCIT_C76126 hasExactSynonym "Adverse Event Without Identified Device or Use Problem" @default.
- NCIT_C76126 hasExactSynonym "Adverse Event without Identified Device or Use Problem" @default.
- NCIT_C76126 inSubset NCIT_C54451 @default.
- NCIT_C76126 inSubset NCIT_C62596 @default.
- NCIT_C76126 type Class @default.
- NCIT_C76126 isDefinedBy ncit.owl @default.
- NCIT_C76126 label "Adverse Event without Identified Device or Use Problem" @default.
- NCIT_C76126 subClassOf NCIT_C20189 @default.
- NCIT_C76126 subClassOf NCIT_C27993 @default.
- NCIT_C76126 subClassOf NCIT_C41009 @default.
- NCIT_C76126 subClassOf NCIT_C48655 @default.
- NCIT_C76126 subClassOf NCIT_C76126 @default.