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- NCIT_C84759 IAO_0000115 "An autosomal dominant inherited disorder of porphyrin metabolism caused by deficiency of the enzyme coproporphyrinogen oxidase. It results in neurologic damage and can include abdominal pain, constipation and psychiatric manifestations." @default.
- NCIT_C84759 NCIT_NHC0 "C84759" @default.
- NCIT_C84759 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84759 NCIT_P108 "Hereditary Coproporphyria" @default.
- NCIT_C84759 NCIT_P207 "C0162531" @default.
- NCIT_C84759 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84759 normalizedInformationContent "100" @default.
- NCIT_C84759 referenceCount "1" @default.
- NCIT_C84759 hasExactSynonym "Hereditary Coproporphyria" @default.
- NCIT_C84759 inSubset NCIT_C165258 @default.
- NCIT_C84759 inSubset NCIT_C192842 @default.
- NCIT_C84759 type Class @default.
- NCIT_C84759 isDefinedBy ncit.owl @default.
- NCIT_C84759 label "Hereditary Coproporphyria" @default.
- NCIT_C84759 subClassOf NCIT_C2991 @default.
- NCIT_C84759 subClassOf NCIT_C3235 @default.
- NCIT_C84759 subClassOf NCIT_C4873 @default.
- NCIT_C84759 subClassOf NCIT_C53529 @default.
- NCIT_C84759 subClassOf NCIT_C53543 @default.
- NCIT_C84759 subClassOf NCIT_C53547 @default.
- NCIT_C84759 subClassOf NCIT_C7057 @default.
- NCIT_C84759 subClassOf NCIT_C84759 @default.
- NCIT_C84759 subClassOf NCIT_C97096 @default.