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- NCIT_C189281 IAO_0000115 "An autosomal recessive condition caused by mutation(s) in the CP gene, encoding ceruloplasmin. It is characterized by low concentrations of ceruloplasmin." @default.
- NCIT_C189281 NCIT_NHC0 "C189281" @default.
- NCIT_C189281 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C189281 NCIT_P108 "Aceruloplasminemia" @default.
- NCIT_C189281 NCIT_P207 "C0878682" @default.
- NCIT_C189281 NCIT_P322 "Cellosaurus" @default.
- NCIT_C189281 NCIT_R176 NCIT_C104137 @default.
- NCIT_C189281 NCIT_R176 NCIT_C16612 @default.
- NCIT_C189281 NCIT_R176 NCIT_C21281 @default.
- NCIT_C189281 NCIT_R176 NCIT_C25939 @default.
- NCIT_C189281 normalizedInformationContent "100" @default.
- NCIT_C189281 referenceCount "1" @default.
- NCIT_C189281 hasExactSynonym "Aceruloplasminemia" @default.
- NCIT_C189281 inSubset NCIT_C165258 @default.
- NCIT_C189281 inSubset NCIT_C192842 @default.
- NCIT_C189281 type Class @default.
- NCIT_C189281 isDefinedBy ncit.owl @default.
- NCIT_C189281 label "Aceruloplasminemia" @default.
- NCIT_C189281 subClassOf B4e839f3b40ac9cd6aae0fb86594c3f64 @default.
- NCIT_C189281 subClassOf B6011adf884ce98d31a3964babf4e0234 @default.
- NCIT_C189281 subClassOf NCIT_C189281 @default.
- NCIT_C189281 subClassOf NCIT_C2991 @default.
- NCIT_C189281 subClassOf NCIT_C4873 @default.
- NCIT_C189281 subClassOf NCIT_C53529 @default.
- NCIT_C189281 subClassOf NCIT_C53543 @default.
- NCIT_C189281 subClassOf NCIT_C53547 @default.
- NCIT_C189281 subClassOf NCIT_C7057 @default.