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- B2f84ba3145e5c09019997efc0d8c0ce3 NCIT_P378 "NCI" @default.
- B2f84ba3145e5c09019997efc0d8c0ce3 type Axiom @default.
- B2f84ba3145e5c09019997efc0d8c0ce3 annotatedProperty IAO_0000115 @default.
- B2f84ba3145e5c09019997efc0d8c0ce3 annotatedSource NCIT_C124927 @default.
- B2f84ba3145e5c09019997efc0d8c0ce3 annotatedTarget "Human ATXN2 wild-type allele is located in the vicinity of 12q24.1 and is approximately 147 kb in length. This allele, which encodes ataxin-2 protein, is involved in the regulation of endocytosis of the epidermal growth factor receptor. Mutation of the gene is associated with spinocerebellar ataxia type 2, susceptibility to amyotrophic lateral sclerosis 13 and increased susceptibility for late-onset Parkinson disease." @default.