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- NCIT_C129977 IAO_0000115 "An inherited condition caused by mutation(s) in the SLC25A4 gene, encoding ADP/ATP translocase 1. It is characterized by hypertrophic cardiomyopathy." @default.
- NCIT_C129977 NCIT_NHC0 "C129977" @default.
- NCIT_C129977 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C129977 NCIT_P108 "Mitochondrial DNA Depletion Syndrome 12" @default.
- NCIT_C129977 NCIT_P208 "CL513034" @default.
- NCIT_C129977 NCIT_P322 "Cellosaurus" @default.
- NCIT_C129977 NCIT_R176 NCIT_C16612 @default.
- NCIT_C129977 NCIT_R176 NCIT_C21295 @default.
- NCIT_C129977 NCIT_R176 NCIT_C28533 @default.
- NCIT_C129977 NCIT_R176 NCIT_C37298 @default.
- NCIT_C129977 normalizedInformationContent "100" @default.
- NCIT_C129977 referenceCount "1" @default.
- NCIT_C129977 hasExactSynonym "MTDPS12" @default.
- NCIT_C129977 hasExactSynonym "Mitochondrial DNA Depletion Syndrome 12" @default.
- NCIT_C129977 inSubset NCIT_C165258 @default.
- NCIT_C129977 inSubset NCIT_C192842 @default.
- NCIT_C129977 type Class @default.
- NCIT_C129977 isDefinedBy ncit.owl @default.
- NCIT_C129977 label "Mitochondrial DNA Depletion Syndrome 12" @default.
- NCIT_C129977 subClassOf B5d1c0a33707f492c61916c60b0c146db @default.
- NCIT_C129977 subClassOf Bc4cd6a44875ef4075654bb3a23dc7439 @default.
- NCIT_C129977 subClassOf NCIT_C129977 @default.
- NCIT_C129977 subClassOf NCIT_C185235 @default.
- NCIT_C129977 subClassOf NCIT_C2991 @default.
- NCIT_C129977 subClassOf NCIT_C3235 @default.
- NCIT_C129977 subClassOf NCIT_C34816 @default.
- NCIT_C129977 subClassOf NCIT_C4873 @default.
- NCIT_C129977 subClassOf NCIT_C53529 @default.
- NCIT_C129977 subClassOf NCIT_C53543 @default.
- NCIT_C129977 subClassOf NCIT_C53547 @default.
- NCIT_C129977 subClassOf NCIT_C7057 @default.