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- NCIT_C129866 IAO_0000115 "An autosomal recessive condition caused by mutation(s) in the SLC6A3 gene, encoding sodium-dependent dopamine transporter. It is characterized by Parkinsonian features and has an onset in early infancy." @default.
- NCIT_C129866 NCIT_NHC0 "C129866" @default.
- NCIT_C129866 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C129866 NCIT_P108 "Dopamine Transporter Deficiency Syndrome" @default.
- NCIT_C129866 NCIT_P207 "C2751067" @default.
- NCIT_C129866 NCIT_P322 "Cellosaurus" @default.
- NCIT_C129866 NCIT_R176 NCIT_C113524 @default.
- NCIT_C129866 NCIT_R176 NCIT_C16612 @default.
- NCIT_C129866 NCIT_R176 NCIT_C21295 @default.
- NCIT_C129866 NCIT_R176 NCIT_C28533 @default.
- NCIT_C129866 normalizedInformationContent "100" @default.
- NCIT_C129866 referenceCount "1" @default.
- NCIT_C129866 hasExactSynonym "Dopamine Transporter Deficiency Syndrome" @default.
- NCIT_C129866 hasExactSynonym "PKDYS" @default.
- NCIT_C129866 hasExactSynonym "Parkinsonism-Dystonia, Infantile" @default.
- NCIT_C129866 inSubset NCIT_C165258 @default.
- NCIT_C129866 inSubset NCIT_C192842 @default.
- NCIT_C129866 type Class @default.
- NCIT_C129866 isDefinedBy ncit.owl @default.
- NCIT_C129866 label "Dopamine Transporter Deficiency Syndrome" @default.
- NCIT_C129866 subClassOf B4c1467f260c344d58fc0b05d0295d238 @default.
- NCIT_C129866 subClassOf Bf0e7634b1d25198aa3e66d78ca2a9246 @default.
- NCIT_C129866 subClassOf NCIT_C129866 @default.
- NCIT_C129866 subClassOf NCIT_C28193 @default.
- NCIT_C129866 subClassOf NCIT_C2991 @default.
- NCIT_C129866 subClassOf NCIT_C7057 @default.