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- NCIT_C75454 IAO_0000115 "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.
- NCIT_C75454 NCIT_NHC0 "C75454" @default.
- NCIT_C75454 NCIT_P100 "0607642" @default.
- NCIT_C75454 NCIT_P102 "AJ230819" @default.
- NCIT_C75454 NCIT_P106 "Gene or Genome" @default.
- NCIT_C75454 NCIT_P108 "RAI1 wt Allele" @default.
- NCIT_C75454 NCIT_P207 "C2698933" @default.
- NCIT_C75454 NCIT_P321 "10743" @default.
- NCIT_C75454 NCIT_P366 "RAI1_wt_Allele" @default.
- NCIT_C75454 NCIT_P98 "transcriptional regulator, may be important for embryonal and postnatal development. May play roles in craniofacial development, control of body weight and complex behavioral responses." @default.
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- NCIT_C75454 normalizedInformationContent "100" @default.
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- NCIT_C75454 hasExactSynonym "DKFZP434A139" @default.
- NCIT_C75454 hasExactSynonym "KIAA1820" @default.
- NCIT_C75454 hasExactSynonym "MGC12824" @default.
- NCIT_C75454 hasExactSynonym "RAI1 wt Allele" @default.
- NCIT_C75454 hasExactSynonym "Retinoic Acid Induced 1 wt Allele" @default.
- NCIT_C75454 hasExactSynonym "Retinoic Acid-Induced Gene 1" @default.
- NCIT_C75454 hasExactSynonym "Retinoic Acid-Inducible 1 Gene" @default.
- NCIT_C75454 hasExactSynonym "SMCR" @default.
- NCIT_C75454 hasExactSynonym "SMS" @default.
- NCIT_C75454 hasExactSynonym "Smith-Magenis Syndrome Chromosome Region Gene" @default.
- NCIT_C75454 type Class @default.
- NCIT_C75454 isDefinedBy ncit.owl @default.
- NCIT_C75454 label "RAI1 wt Allele" @default.
- NCIT_C75454 subClassOf NCIT_C16612 @default.
- NCIT_C75454 subClassOf NCIT_C20420 @default.
- NCIT_C75454 subClassOf NCIT_C54362 @default.
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