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- NCIT_C174219 IAO_0000115 "An autosomal dominant type of primary pulmonary hypertension caused by mutation(s) in the BMPR2 gene, encoding bone morphogenetic protein receptor type-2." @default.
- NCIT_C174219 NCIT_NHC0 "C174219" @default.
- NCIT_C174219 NCIT_P106 "Finding" @default.
- NCIT_C174219 NCIT_P108 "Primary Pulmonary Hypertension-1" @default.
- NCIT_C174219 NCIT_P208 "CL1411774" @default.
- NCIT_C174219 NCIT_P322 "Cellosaurus" @default.
- NCIT_C174219 normalizedInformationContent "100" @default.
- NCIT_C174219 referenceCount "1" @default.
- NCIT_C174219 hasExactSynonym "PPH1" @default.
- NCIT_C174219 hasExactSynonym "Primary Pulmonary Hypertension-1" @default.
- NCIT_C174219 inSubset NCIT_C165258 @default.
- NCIT_C174219 inSubset NCIT_C192842 @default.
- NCIT_C174219 type Class @default.
- NCIT_C174219 isDefinedBy ncit.owl @default.
- NCIT_C174219 label "Primary Pulmonary Hypertension-1" @default.
- NCIT_C174219 subClassOf NCIT_C168400 @default.
- NCIT_C174219 subClassOf NCIT_C173902 @default.
- NCIT_C174219 subClassOf NCIT_C174219 @default.
- NCIT_C174219 subClassOf NCIT_C3117 @default.
- NCIT_C174219 subClassOf NCIT_C3120 @default.
- NCIT_C174219 subClassOf NCIT_C3367 @default.
- NCIT_C174219 subClassOf NCIT_C35552 @default.
- NCIT_C174219 subClassOf NCIT_C36278 @default.
- NCIT_C174219 subClassOf NCIT_C36295 @default.
- NCIT_C174219 subClassOf NCIT_C54707 @default.
- NCIT_C174219 subClassOf NCIT_C7057 @default.