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- NCIT_C75422 IAO_0000115 "Human FMR1 wild-type allele is located in the vicinity of Xq27.3 and is approximately 39 kb in length. This allele, which encodes fragile X mental retardation protein 1, may play a role in the mediation of mRNA transport. Amplification of a trinucleotide repeat (CGG) within the gene is associated with fragile X syndrome." @default.
- NCIT_C75422 NCIT_NHC0 "C75422" @default.
- NCIT_C75422 NCIT_P100 "309550" @default.
- NCIT_C75422 NCIT_P102 "X69962" @default.
- NCIT_C75422 NCIT_P106 "Gene or Genome" @default.
- NCIT_C75422 NCIT_P108 "FMR1 wt Allele" @default.
- NCIT_C75422 NCIT_P207 "C2700049" @default.
- NCIT_C75422 NCIT_P321 "2332" @default.
- NCIT_C75422 NCIT_P366 "FMR1_wt_Allele" @default.
- NCIT_C75422 NCIT_P98 "Fragile X tremor/ataxia syndrome results from the occurrence of 55-200 repeats of the CGG sequence while having over 200 repeats of the trinucleotide results in the more severe fragile X syndrome with mental retardation." @default.
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- NCIT_C75422 normalizedInformationContent "100" @default.
- NCIT_C75422 referenceCount "1" @default.
- NCIT_C75422 hasExactSynonym "FMR1 wt Allele" @default.
- NCIT_C75422 hasExactSynonym "FMRP" @default.
- NCIT_C75422 hasExactSynonym "FRAXA" @default.
- NCIT_C75422 hasExactSynonym "Fragile X Mental Retardation 1 wt Allele" @default.
- NCIT_C75422 hasExactSynonym "MGC87458" @default.
- NCIT_C75422 hasExactSynonym "POF" @default.
- NCIT_C75422 hasExactSynonym "POF1" @default.
- NCIT_C75422 hasExactSynonym "Premature Ovarian Failure 1 Gene" @default.
- NCIT_C75422 type Class @default.
- NCIT_C75422 isDefinedBy ncit.owl @default.
- NCIT_C75422 label "FMR1 wt Allele" @default.
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