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- NCIT_C84729 IAO_0000115 "An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice." @default.
- NCIT_C84729 NCIT_A32 NCIT_C17103 @default.
- NCIT_C84729 NCIT_NHC0 "C84729" @default.
- NCIT_C84729 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84729 NCIT_P108 "Gilbert Syndrome" @default.
- NCIT_C84729 NCIT_P207 "C0017551" @default.
- NCIT_C84729 NCIT_P322 "GDC" @default.
- NCIT_C84729 NCIT_P375 "Gilbert's Syndrome" @default.
- NCIT_C84729 NCIT_R176 NCIT_C16612 @default.
- NCIT_C84729 NCIT_R176 NCIT_C20128 @default.
- NCIT_C84729 NCIT_R176 NCIT_C21281 @default.
- NCIT_C84729 NCIT_R176 NCIT_C25870 @default.
- NCIT_C84729 NCIT_R176 NCIT_C26147 @default.
- NCIT_C84729 normalizedInformationContent "100" @default.
- NCIT_C84729 referenceCount "1" @default.
- NCIT_C84729 hasExactSynonym "Gilbert Disease" @default.
- NCIT_C84729 hasExactSynonym "Gilbert Syndrome" @default.
- NCIT_C84729 hasExactSynonym "Gilbert's Syndrome" @default.
- NCIT_C84729 inSubset NCIT_C157711 @default.
- NCIT_C84729 inSubset NCIT_C177537 @default.
- NCIT_C84729 type Class @default.
- NCIT_C84729 isDefinedBy ncit.owl @default.
- NCIT_C84729 label "Gilbert Syndrome" @default.
- NCIT_C84729 subClassOf B47a95c116a16baa84478f4f46a3ffada @default.
- NCIT_C84729 subClassOf Bd340467f0b7ccb41827f99d0435d71c4 @default.
- NCIT_C84729 subClassOf NCIT_C28193 @default.
- NCIT_C84729 subClassOf NCIT_C2991 @default.
- NCIT_C84729 subClassOf NCIT_C3235 @default.
- NCIT_C84729 subClassOf NCIT_C34816 @default.
- NCIT_C84729 subClassOf NCIT_C4873 @default.
- NCIT_C84729 subClassOf NCIT_C53529 @default.
- NCIT_C84729 subClassOf NCIT_C53543 @default.
- NCIT_C84729 subClassOf NCIT_C53547 @default.
- NCIT_C84729 subClassOf NCIT_C7057 @default.
- NCIT_C84729 subClassOf NCIT_C84729 @default.
- NCIT_C84729 subClassOf NCIT_C84761 @default.