Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C84756> ?p ?o ?g. }
Showing items 1 to 35 of
35
with 100 items per page.
- NCIT_C84756 IAO_0000115 "A rare autosomal recessive inherited disorder caused by mutations in the ATP7B gene. It is characterized by copper accumulation in the tissues, particularly brain and liver. It results in liver failure, neurologic, and psychotic manifestations." @default.
- NCIT_C84756 NCIT_A13 NCIT_C177192 @default.
- NCIT_C84756 NCIT_NHC0 "C84756" @default.
- NCIT_C84756 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84756 NCIT_P108 "Hepatolenticular Degeneration" @default.
- NCIT_C84756 NCIT_P207 "C0019202" @default.
- NCIT_C84756 NCIT_P322 "CCPS" @default.
- NCIT_C84756 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84756 NCIT_R176 NCIT_C158414 @default.
- NCIT_C84756 NCIT_R176 NCIT_C16612 @default.
- NCIT_C84756 NCIT_R176 NCIT_C177192 @default.
- NCIT_C84756 NCIT_R176 NCIT_C21281 @default.
- NCIT_C84756 NCIT_R176 NCIT_C21295 @default.
- NCIT_C84756 NCIT_R176 NCIT_C28533 @default.
- NCIT_C84756 normalizedInformationContent "100" @default.
- NCIT_C84756 referenceCount "1" @default.
- NCIT_C84756 hasExactSynonym "Hepatolenticular Degeneration" @default.
- NCIT_C84756 hasExactSynonym "Wilson Disease" @default.
- NCIT_C84756 hasExactSynonym "Wilson's Disease" @default.
- NCIT_C84756 inSubset NCIT_C165258 @default.
- NCIT_C84756 inSubset NCIT_C177281 @default.
- NCIT_C84756 inSubset NCIT_C177516 @default.
- NCIT_C84756 inSubset NCIT_C192842 @default.
- NCIT_C84756 type Class @default.
- NCIT_C84756 isDefinedBy ncit.owl @default.
- NCIT_C84756 label "Hepatolenticular Degeneration" @default.
- NCIT_C84756 subClassOf Bcecdf192b75cd3d52ac6ada6521adeaa @default.
- NCIT_C84756 subClassOf Be1cecd18ff22970f69ffc6c908c7e01e @default.
- NCIT_C84756 subClassOf NCIT_C2991 @default.
- NCIT_C84756 subClassOf NCIT_C4873 @default.
- NCIT_C84756 subClassOf NCIT_C53529 @default.
- NCIT_C84756 subClassOf NCIT_C53543 @default.
- NCIT_C84756 subClassOf NCIT_C53547 @default.
- NCIT_C84756 subClassOf NCIT_C7057 @default.
- NCIT_C84756 subClassOf NCIT_C84756 @default.