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- NCIT_C128806 IAO_0000115 "An autosomal dominant genetic condition caused by mutation(s) in the CETP gene, encoding cholesteryl ester transfer protein. Affected individuals may have increased longevity due to decreased risk of coronary heart disease." @default.
- NCIT_C128806 NCIT_NHC0 "C128806" @default.
- NCIT_C128806 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C128806 NCIT_P108 "Hyperalphalipoproteinemia" @default.
- NCIT_C128806 NCIT_P207 "C0342883" @default.
- NCIT_C128806 NCIT_R176 NCIT_C16612 @default.
- NCIT_C128806 NCIT_R176 NCIT_C21295 @default.
- NCIT_C128806 NCIT_R176 NCIT_C28533 @default.
- NCIT_C128806 NCIT_R176 NCIT_C39780 @default.
- NCIT_C128806 normalizedInformationContent "100" @default.
- NCIT_C128806 referenceCount "1" @default.
- NCIT_C128806 hasExactSynonym "HALP1" @default.
- NCIT_C128806 hasExactSynonym "Hyperalphalipoproteinemia" @default.
- NCIT_C128806 type Class @default.
- NCIT_C128806 isDefinedBy ncit.owl @default.
- NCIT_C128806 label "Hyperalphalipoproteinemia" @default.
- NCIT_C128806 subClassOf B33e5d1b5651212bf038a35b00647987b @default.
- NCIT_C128806 subClassOf B8ba4d7d44e069a9926aa52104341bf5c @default.
- NCIT_C128806 subClassOf NCIT_C128806 @default.
- NCIT_C128806 subClassOf NCIT_C2991 @default.
- NCIT_C128806 subClassOf NCIT_C3235 @default.
- NCIT_C128806 subClassOf NCIT_C34709 @default.
- NCIT_C128806 subClassOf NCIT_C53529 @default.
- NCIT_C128806 subClassOf NCIT_C53547 @default.
- NCIT_C128806 subClassOf NCIT_C7057 @default.