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- NCIT_C75471 IAO_0000115 "A group of connective tissue disorder caused by mutations in the COL1A1 gene mapped to chromosome 17q21. It includes the Ehlers-Danlos syndrome, osteogenesis imperfecta, and osteoporosis." @default.
- NCIT_C75471 NCIT_A13 NCIT_C29949 @default.
- NCIT_C75471 NCIT_NHC0 "C75471" @default.
- NCIT_C75471 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C75471 NCIT_P108 "COL1A1 Associated Connective Tissue Disorder" @default.
- NCIT_C75471 NCIT_P207 "C0268331" @default.
- NCIT_C75471 NCIT_P366 "COL1A1_Associated_Connective_Tissue_Disorder" @default.
- NCIT_C75471 NCIT_R100 NCIT_C12219 @default.
- NCIT_C75471 NCIT_R100 NCIT_C12366 @default.
- NCIT_C75471 NCIT_R100 NCIT_C12801 @default.
- NCIT_C75471 NCIT_R100 NCIT_C12964 @default.
- NCIT_C75471 NCIT_R100 NCIT_C25769 @default.
- NCIT_C75471 NCIT_R100 NCIT_C32221 @default.
- NCIT_C75471 NCIT_R100 NCIT_C34076 @default.
- NCIT_C75471 normalizedInformationContent "79.546070929969886" @default.
- NCIT_C75471 referenceCount "22" @default.
- NCIT_C75471 hasExactSynonym "COL1A1 Associated Connective Tissue Disorder" @default.
- NCIT_C75471 type Class @default.
- NCIT_C75471 isDefinedBy ncit.owl @default.
- NCIT_C75471 label "COL1A1 Associated Connective Tissue Disorder" @default.
- NCIT_C75471 subClassOf NCIT_C26729 @default.
- NCIT_C75471 subClassOf NCIT_C27551 @default.
- NCIT_C75471 subClassOf NCIT_C27574 @default.
- NCIT_C75471 subClassOf NCIT_C2991 @default.
- NCIT_C75471 subClassOf NCIT_C7057 @default.
- NCIT_C75471 subClassOf NCIT_C75471 @default.
- NCIT_C75471 subClassOf NCIT_C97075 @default.