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- NCIT_C178382 IAO_0000115 "A group of autosomal dominant-inherited disorders caused by mutation(s) in the CDC73 gene, encoding parafibromin. These disorders are associated with hyperparathyroidism secondary to parathyroid neoplasms." @default.
- NCIT_C178382 NCIT_A13 NCIT_C43569 @default.
- NCIT_C178382 NCIT_NHC0 "C178382" @default.
- NCIT_C178382 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C178382 NCIT_P108 "CDC73-Related Neoplastic Syndrome" @default.
- NCIT_C178382 NCIT_P208 "CL1647853" @default.
- NCIT_C178382 NCIT_P322 "CCPS" @default.
- NCIT_C178382 NCIT_R108 NCIT_C3367 @default.
- NCIT_C178382 NCIT_R108 NCIT_C3824 @default.
- NCIT_C178382 NCIT_R108 NCIT_C54062 @default.
- NCIT_C178382 NCIT_R108 NCIT_C7057 @default.
- NCIT_C178382 NCIT_R176 NCIT_C16612 @default.
- NCIT_C178382 NCIT_R176 NCIT_C43569 @default.
- NCIT_C178382 NCIT_R176 NCIT_C54362 @default.
- NCIT_C178382 normalizedInformationContent "89.350088392419622" @default.
- NCIT_C178382 referenceCount "5" @default.
- NCIT_C178382 hasExactSynonym "CDC73-Related Neoplastic Syndrome" @default.
- NCIT_C178382 inSubset NCIT_C177281 @default.
- NCIT_C178382 inSubset NCIT_C177516 @default.
- NCIT_C178382 type Class @default.
- NCIT_C178382 isDefinedBy ncit.owl @default.
- NCIT_C178382 label "CDC73-Related Neoplastic Syndrome" @default.
- NCIT_C178382 subClassOf B55ec09347d4163417609d935d77d8486 @default.
- NCIT_C178382 subClassOf Bba741d36c1b2ccf6c27b3dc8831c471d @default.
- NCIT_C178382 subClassOf NCIT_C178382 @default.
- NCIT_C178382 subClassOf NCIT_C28193 @default.
- NCIT_C178382 subClassOf NCIT_C2991 @default.
- NCIT_C178382 subClassOf NCIT_C3101 @default.
- NCIT_C178382 subClassOf NCIT_C3266 @default.
- NCIT_C178382 subClassOf NCIT_C54705 @default.
- NCIT_C178382 subClassOf NCIT_C7057 @default.