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- Bb9dc1043af0b7d7c1be0b0fe121b2eb4 NCIT_P378 "NCI" @default.
- Bb9dc1043af0b7d7c1be0b0fe121b2eb4 type Axiom @default.
- Bb9dc1043af0b7d7c1be0b0fe121b2eb4 annotatedProperty IAO_0000115 @default.
- Bb9dc1043af0b7d7c1be0b0fe121b2eb4 annotatedSource NCIT_C84413 @default.
- Bb9dc1043af0b7d7c1be0b0fe121b2eb4 annotatedTarget "Human SIX1 wild-type allele is located in the vicinity of 14q23.1 and is approximately 3 kb in length. This allele, which encodes homeobox protein SIX1, may play a role in skeletal muscle development. Mutation of the gene is associated with both autosomal dominant deafness type 23 and branchiootic syndrome type 3." @default.