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- NCIT_C198608 IAO_0000115 "An autosomal recessive subtype of Parkinson disease, caused by mutation(s) in the DNAJC6 gene, encoding putative tyrosine-protein phosphatase auxilin. It is characterized by an onset of Parkinsonism in the first or second decade. Mutations(s) in DNAJC6, are also causative in PARK19B." @default.
- NCIT_C198608 NCIT_NHC0 "C198608" @default.
- NCIT_C198608 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C198608 NCIT_P108 "Parkinson Disease 19A, Juvenile-Onset" @default.
- NCIT_C198608 NCIT_P322 "Cellosaurus" @default.
- NCIT_C198608 NCIT_R100 NCIT_C12219 @default.
- NCIT_C198608 NCIT_R100 NCIT_C12438 @default.
- NCIT_C198608 NCIT_R100 NCIT_C12755 @default.
- NCIT_C198608 NCIT_R100 NCIT_C12919 @default.
- NCIT_C198608 NCIT_R100 NCIT_C13040 @default.
- NCIT_C198608 NCIT_R100 NCIT_C32221 @default.
- NCIT_C198608 normalizedInformationContent "100" @default.
- NCIT_C198608 referenceCount "1" @default.
- NCIT_C198608 hasExactSynonym "PARK19A" @default.
- NCIT_C198608 hasExactSynonym "Parkinson Disease 19A, Juvenile-Onset" @default.
- NCIT_C198608 inSubset NCIT_C165258 @default.
- NCIT_C198608 inSubset NCIT_C192842 @default.
- NCIT_C198608 type Class @default.
- NCIT_C198608 isDefinedBy ncit.owl @default.
- NCIT_C198608 label "Parkinson Disease 19A, Juvenile-Onset" @default.
- NCIT_C198608 subClassOf NCIT_C198608 @default.
- NCIT_C198608 subClassOf NCIT_C26835 @default.
- NCIT_C198608 subClassOf NCIT_C26845 @default.
- NCIT_C198608 subClassOf NCIT_C27090 @default.
- NCIT_C198608 subClassOf NCIT_C27551 @default.
- NCIT_C198608 subClassOf NCIT_C27586 @default.
- NCIT_C198608 subClassOf NCIT_C27588 @default.
- NCIT_C198608 subClassOf NCIT_C2934 @default.
- NCIT_C198608 subClassOf NCIT_C2991 @default.
- NCIT_C198608 subClassOf NCIT_C4802 @default.
- NCIT_C198608 subClassOf NCIT_C53529 @default.
- NCIT_C198608 subClassOf NCIT_C53531 @default.
- NCIT_C198608 subClassOf NCIT_C53547 @default.
- NCIT_C198608 subClassOf NCIT_C7057 @default.
- NCIT_C198608 subClassOf NCIT_C79593 @default.