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- NCIT_C43755 IAO_0000115 "A role used to relate a disease to the type of chromosomal abnormality present in the specified disease state. The domain and the range for this role are 'Disease, Disorder or Finding' and 'Molecular Abnormality', respectively." @default.
- NCIT_C43755 NCIT_A1 NCIT_C7057 @default.
- NCIT_C43755 NCIT_A2 NCIT_C3910 @default.
- NCIT_C43755 NCIT_NHC0 "C43755" @default.
- NCIT_C43755 NCIT_P106 "Conceptual Entity" @default.
- NCIT_C43755 NCIT_P107 "Has Cytogenetic Abnormality" @default.
- NCIT_C43755 NCIT_P108 "Disease_Has_Cytogenetic_Abnormality" @default.
- NCIT_C43755 NCIT_P207 "C1707774" @default.
- NCIT_C43755 NCIT_P366 "Disease_Has_Cytogenetic_Abnormality_Role" @default.
- NCIT_C43755 normalizedInformationContent "100" @default.
- NCIT_C43755 referenceCount "1" @default.
- NCIT_C43755 hasExactSynonym "Disease_Has_Cytogenetic_Abnormality" @default.
- NCIT_C43755 type Class @default.
- NCIT_C43755 isDefinedBy ncit.owl @default.
- NCIT_C43755 label "obsolete Disease_Has_Cytogenetic_Abnormality" @default.
- NCIT_C43755 subClassOf NCIT_C43755 @default.
- NCIT_C43755 subClassOf Thing @default.
- NCIT_C43755 deprecated "true" @default.