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- NCIT_C103966 IAO_0000115 "Human ACTB wild-type allele is located in the vicinity of 7p22 and is approximately 37 kb in length. This allele, which encodes actin, cytoplasmic 1 protein, plays a role in the modulation of both cell motility and cell shape. Mutation of the gene is associated with dystonia juvenile-onset and Baraitser-Winter syndrome type 1." @default.
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- NCIT_C103966 NCIT_P106 "Gene or Genome" @default.
- NCIT_C103966 NCIT_P107 "ACTB wt Allele" @default.
- NCIT_C103966 NCIT_P108 "ACTB wt Allele" @default.
- NCIT_C103966 NCIT_P207 "C3541874" @default.
- NCIT_C103966 NCIT_P321 "60" @default.
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- NCIT_C103966 normalizedInformationContent "100" @default.
- NCIT_C103966 referenceCount "1" @default.
- NCIT_C103966 hasExactSynonym "ACTB wt Allele" @default.
- NCIT_C103966 hasExactSynonym "Actin, Beta wt Allele" @default.
- NCIT_C103966 hasExactSynonym "BRWS1" @default.
- NCIT_C103966 hasExactSynonym "PS1TP5BP1" @default.
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- NCIT_C103966 type Class @default.
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- NCIT_C103966 label "ACTB wt Allele" @default.
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