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- NCIT_C41333 IAO_0000115 "Any adverse event associated with a medical product or procedure, whose nature and severity have been previously observed, identified in nature, severity, or frequency, and documented in the investigator brochure, investigational plan, protocol, current consent form, scientific publication, or in other relevant and reliable document. The old term Side Effect is retired and should not be used." @default.
- NCIT_C41333 NCIT_NHC0 "C41333" @default.
- NCIT_C41333 NCIT_P106 "Finding" @default.
- NCIT_C41333 NCIT_P108 "Expected Adverse Event" @default.
- NCIT_C41333 NCIT_P207 "C1517002" @default.
- NCIT_C41333 NCIT_P322 "PCDC" @default.
- NCIT_C41333 NCIT_P366 "Expected_Adverse_Event" @default.
- NCIT_C41333 normalizedInformationContent "100" @default.
- NCIT_C41333 referenceCount "1" @default.
- NCIT_C41333 hasExactSynonym "EAE" @default.
- NCIT_C41333 hasExactSynonym "Expected Adverse Event" @default.
- NCIT_C41333 hasExactSynonym "Expected" @default.
- NCIT_C41333 inSubset NCIT_C186334 @default.
- NCIT_C41333 inSubset NCIT_C186341 @default.
- NCIT_C41333 type Class @default.
- NCIT_C41333 isDefinedBy ncit.owl @default.
- NCIT_C41333 label "Expected Adverse Event" @default.
- NCIT_C41333 subClassOf NCIT_C154678 @default.
- NCIT_C41333 subClassOf NCIT_C3367 @default.
- NCIT_C41333 subClassOf NCIT_C36291 @default.
- NCIT_C41333 subClassOf NCIT_C41331 @default.
- NCIT_C41333 subClassOf NCIT_C41333 @default.
- NCIT_C41333 subClassOf NCIT_C7057 @default.