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- NCIT_C201156 IAO_0000115 "Human FAM111A wild-type allele is located in the vicinity of 11q12.1 and is approximately 12 kb in length. This allele, which encodes serine protease FAM111A protein, plays a role in the repair of DNA-protein crosslinks. Mutations in the gene are associated with both Gracile bone dysplasia and Kenny-Caffey syndrome 2." @default.
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- NCIT_C201156 NCIT_P106 "Gene or Genome" @default.
- NCIT_C201156 NCIT_P108 "FAM111A wt Allele" @default.
- NCIT_C201156 NCIT_P321 "63901" @default.
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- NCIT_C201156 normalizedInformationContent "100" @default.
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- NCIT_C201156 hasExactSynonym "FAM111 Trypsin Like Peptidase A wt Allele" @default.
- NCIT_C201156 hasExactSynonym "FAM111A wt Allele" @default.
- NCIT_C201156 hasExactSynonym "FLJ22794" @default.
- NCIT_C201156 hasExactSynonym "Family With Sequence Similarity 111 Member A Gene" @default.
- NCIT_C201156 hasExactSynonym "GCLEB" @default.
- NCIT_C201156 hasExactSynonym "KCS2" @default.
- NCIT_C201156 hasExactSynonym "KIAA1895" @default.
- NCIT_C201156 type Class @default.
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- NCIT_C201156 label "FAM111A wt Allele" @default.
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