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- NCIT_C86554 IAO_0000115 "Human FANCF wild-type allele is located in the vicinity of 11p15 and is approximately 3 kb in length. This allele, which encodes Fanconi anemia group F protein, may play a role in the modulation of both cell cycle progression and DNA repair. Mutation of the gene is associated with Fanconi anemia." @default.
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- NCIT_C86554 NCIT_P102 "NM_022725" @default.
- NCIT_C86554 NCIT_P106 "Gene or Genome" @default.
- NCIT_C86554 NCIT_P107 "FANCF wt Allele" @default.
- NCIT_C86554 NCIT_P108 "FANCF wt Allele" @default.
- NCIT_C86554 NCIT_P207 "C2828056" @default.
- NCIT_C86554 NCIT_P321 "2188" @default.
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- NCIT_C86554 normalizedInformationContent "100" @default.
- NCIT_C86554 referenceCount "1" @default.
- NCIT_C86554 hasExactSynonym "FA Complementation Group F wt Allele" @default.
- NCIT_C86554 hasExactSynonym "FAF" @default.
- NCIT_C86554 hasExactSynonym "FANCF wt Allele" @default.
- NCIT_C86554 hasExactSynonym "Fanconi Anemia Complementation Group F Gene" @default.
- NCIT_C86554 hasExactSynonym "Fanconi Anemia, Complementation Group F Gene" @default.
- NCIT_C86554 hasExactSynonym "MGC126856" @default.
- NCIT_C86554 inSubset NCIT_C116977 @default.
- NCIT_C86554 inSubset NCIT_C142799 @default.
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- NCIT_C86554 type Class @default.
- NCIT_C86554 isDefinedBy ncit.owl @default.
- NCIT_C86554 label "FANCF wt Allele" @default.
- NCIT_C86554 subClassOf NCIT_C159207 @default.
- NCIT_C86554 subClassOf NCIT_C16612 @default.
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