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- NCIT_C172392 IAO_0000115 "An inherited ciliary motility defect caused by mutation(s) in the DNAH5 gene, encoding dynein heavy chain 5, axonemal." @default.
- NCIT_C172392 NCIT_NHC0 "C172392" @default.
- NCIT_C172392 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C172392 NCIT_P108 "Primary Ciliary Dyskinesia 3" @default.
- NCIT_C172392 NCIT_P207 "C1837618" @default.
- NCIT_C172392 NCIT_P322 "Cellosaurus" @default.
- NCIT_C172392 NCIT_R176 NCIT_C16612 @default.
- NCIT_C172392 NCIT_R176 NCIT_C200784 @default.
- NCIT_C172392 NCIT_R176 NCIT_C20744 @default.
- NCIT_C172392 NCIT_R176 NCIT_C20745 @default.
- NCIT_C172392 normalizedInformationContent "100" @default.
- NCIT_C172392 referenceCount "1" @default.
- NCIT_C172392 hasExactSynonym "CILD3" @default.
- NCIT_C172392 hasExactSynonym "Primary Ciliary Dyskinesia 3" @default.
- NCIT_C172392 inSubset NCIT_C165258 @default.
- NCIT_C172392 inSubset NCIT_C192842 @default.
- NCIT_C172392 type Class @default.
- NCIT_C172392 isDefinedBy ncit.owl @default.
- NCIT_C172392 label "Primary Ciliary Dyskinesia 3" @default.
- NCIT_C172392 subClassOf B04b1e76dc51e529b627daa091e0c5112 @default.
- NCIT_C172392 subClassOf Ba77c2201de1d789ba9900f8059307cf0 @default.
- NCIT_C172392 subClassOf NCIT_C172392 @default.
- NCIT_C172392 subClassOf NCIT_C2991 @default.
- NCIT_C172392 subClassOf NCIT_C4873 @default.
- NCIT_C172392 subClassOf NCIT_C53529 @default.
- NCIT_C172392 subClassOf NCIT_C53543 @default.
- NCIT_C172392 subClassOf NCIT_C53547 @default.
- NCIT_C172392 subClassOf NCIT_C7057 @default.
- NCIT_C172392 subClassOf NCIT_C84638 @default.