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- NCIT_C102937 IAO_0000115 "Human SNCAIP wild-type allele is located in the vicinity of 5q23.2 and is approximately 153 kb in length. This allele, which encodes synphilin-1 protein, plays a role in the regulation of protein ubiquitination. Mutation of the gene may be associated with Parkinson disease." @default.
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- NCIT_C102937 NCIT_P106 "Gene or Genome" @default.
- NCIT_C102937 NCIT_P107 "SNCAIP wt Allele" @default.
- NCIT_C102937 NCIT_P108 "SNCAIP wt Allele" @default.
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- NCIT_C102937 NCIT_P321 "9627" @default.
- NCIT_C102937 NCIT_P322 "CTRP" @default.
- NCIT_C102937 NCIT_P98 "Tandem duplication of the SNCAIP gene is associated with subgroup 4 medulloblastoma. (Nature. 2012; 488:49-56.)" @default.
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- NCIT_C102937 hasExactSynonym "SNCAIP wt Allele" @default.
- NCIT_C102937 hasExactSynonym "SYPH1" @default.
- NCIT_C102937 hasExactSynonym "Sph1" @default.
- NCIT_C102937 hasExactSynonym "Synuclein, Alpha Interacting Protein wt Allele" @default.
- NCIT_C102937 inSubset NCIT_C116977 @default.
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- NCIT_C102937 type Class @default.
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- NCIT_C102937 label "SNCAIP wt Allele" @default.
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