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- NCIT_C179057 IAO_0000115 "An autosomal recessive subtype of primary hypertrophic osteoarthropathy caused by mutation(s) in the HPGD gene, encoding 15-hydroxyprostaglandin dehydrogenase [NAD+]." @default.
- NCIT_C179057 NCIT_NHC0 "C179057" @default.
- NCIT_C179057 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C179057 NCIT_P108 "Primary Hypertrophic Osteoarthropathy, Autosomal Recessive Type 1" @default.
- NCIT_C179057 NCIT_P208 "CL1648555" @default.
- NCIT_C179057 NCIT_P322 "Cellosaurus" @default.
- NCIT_C179057 NCIT_R176 NCIT_C16612 @default.
- NCIT_C179057 NCIT_R176 NCIT_C21281 @default.
- NCIT_C179057 NCIT_R176 NCIT_C25939 @default.
- NCIT_C179057 NCIT_R176 NCIT_C78137 @default.
- NCIT_C179057 normalizedInformationContent "100" @default.
- NCIT_C179057 referenceCount "1" @default.
- NCIT_C179057 hasExactSynonym "PHOAR1" @default.
- NCIT_C179057 hasExactSynonym "Primary Hypertrophic Osteoarthropathy, Autosomal Recessive Type 1" @default.
- NCIT_C179057 inSubset NCIT_C165258 @default.
- NCIT_C179057 inSubset NCIT_C192842 @default.
- NCIT_C179057 type Class @default.
- NCIT_C179057 isDefinedBy ncit.owl @default.
- NCIT_C179057 label "Primary Hypertrophic Osteoarthropathy, Autosomal Recessive Type 1" @default.
- NCIT_C179057 subClassOf Ba1788c53e518c0b8820cce69331cb8f1 @default.
- NCIT_C179057 subClassOf Bb1c7a8544bac5168b5346bb4adc79d55 @default.
- NCIT_C179057 subClassOf NCIT_C179057 @default.
- NCIT_C179057 subClassOf NCIT_C2991 @default.
- NCIT_C179057 subClassOf NCIT_C4873 @default.
- NCIT_C179057 subClassOf NCIT_C53529 @default.
- NCIT_C179057 subClassOf NCIT_C53543 @default.
- NCIT_C179057 subClassOf NCIT_C53547 @default.
- NCIT_C179057 subClassOf NCIT_C7057 @default.
- NCIT_C179057 subClassOf NCIT_C85023 @default.