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- NCIT_C139458 IAO_0000115 "The investigation involved the analysis of relevant information provided by the user (e.g. healthcare professional, patient, clinical engineer) or a third party (e.g. testing facility) in view of supporting the identification of possible causes for the adverse event." @default.
- NCIT_C139458 NCIT_NHC0 "C139458" @default.
- NCIT_C139458 NCIT_P106 "Functional Concept" @default.
- NCIT_C139458 NCIT_P108 "Analysis of Information Provided by User/Third Party" @default.
- NCIT_C139458 NCIT_P208 "CL526760" @default.
- NCIT_C139458 NCIT_P322 "FDA" @default.
- NCIT_C139458 NCIT_P325 "The investigation involved the analysis of relevant information provided by the user (e.g. healthcare professional, patient, clinical engineer) or a third party (e.g. testing facility) in view of supporting the identification of possible causes for the adverse event. This does not include information recorded by the device." @default.
- NCIT_C139458 normalizedInformationContent "100" @default.
- NCIT_C139458 referenceCount "1" @default.
- NCIT_C139458 hasDbXref "IMDRF:B15" @default.
- NCIT_C139458 hasExactSynonym "Analysis of Information Provided by User/Third Party" @default.
- NCIT_C139458 inSubset NCIT_C62596 @default.
- NCIT_C139458 inSubset NCIT_C91800 @default.
- NCIT_C139458 type Class @default.
- NCIT_C139458 isDefinedBy ncit.owl @default.
- NCIT_C139458 label "Analysis of Information Provided by User/Third Party" @default.
- NCIT_C139458 subClassOf NCIT_C139458 @default.
- NCIT_C139458 subClassOf NCIT_C43431 @default.
- NCIT_C139458 subClassOf NCIT_C49235 @default.
- NCIT_C139458 subClassOf NCIT_C53590 @default.
- NCIT_C139458 subClassOf NCIT_C53648 @default.
- NCIT_C139458 subClassOf NCIT_C54028 @default.
- NCIT_C139458 subClassOf NCIT_C54343 @default.