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- B3c5def0b926b0b61599d68c68fc153ac NCIT_P378 "NCI" @default.
- B3c5def0b926b0b61599d68c68fc153ac type Axiom @default.
- B3c5def0b926b0b61599d68c68fc153ac annotatedProperty IAO_0000115 @default.
- B3c5def0b926b0b61599d68c68fc153ac annotatedSource NCIT_C75454 @default.
- B3c5def0b926b0b61599d68c68fc153ac annotatedTarget "Human RAI1 wild-type allele is located in the vicinity of 17p11.2 and is approximately 130 kb in length. This allele, which encodes retinoic acid-induced protein 1, plays roles in transcriptional regulation, development, control of body weight and complex behavioral responses. Mutations in this gene are associated with Smith-Magenis Syndrome." @default.