Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C84697> ?p ?o ?g. }
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- NCIT_C84697 IAO_0000115 "A rare congenital metabolic disorder characterized by an inborn error of porphyrin-heme biosynthesis. It is caused by deficiency of the enzyme uroporphyrinogen III cosynthetase. It results in cutaneous photosensitivity leading to blistering and scarring of the exposed skin areas." @default.
- NCIT_C84697 NCIT_NHC0 "C84697" @default.
- NCIT_C84697 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84697 NCIT_P108 "Erythropoietic Porphyria" @default.
- NCIT_C84697 NCIT_P207 "C0162530" @default.
- NCIT_C84697 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84697 normalizedInformationContent "100" @default.
- NCIT_C84697 referenceCount "1" @default.
- NCIT_C84697 hasExactSynonym "CEP" @default.
- NCIT_C84697 hasExactSynonym "Erythropoietic Porphyria" @default.
- NCIT_C84697 inSubset NCIT_C165258 @default.
- NCIT_C84697 inSubset NCIT_C192842 @default.
- NCIT_C84697 type Class @default.
- NCIT_C84697 isDefinedBy ncit.owl @default.
- NCIT_C84697 label "Erythropoietic Porphyria" @default.
- NCIT_C84697 subClassOf NCIT_C2991 @default.
- NCIT_C84697 subClassOf NCIT_C3235 @default.
- NCIT_C84697 subClassOf NCIT_C4873 @default.
- NCIT_C84697 subClassOf NCIT_C53529 @default.
- NCIT_C84697 subClassOf NCIT_C53543 @default.
- NCIT_C84697 subClassOf NCIT_C53547 @default.
- NCIT_C84697 subClassOf NCIT_C7057 @default.
- NCIT_C84697 subClassOf NCIT_C84697 @default.
- NCIT_C84697 subClassOf NCIT_C97096 @default.