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- NCIT_C86552 IAO_0000115 "Human FANCE wild-type allele is located within 6p22-p21 and is approximately 15 kb in length. This allele, which encodes Fanconi anemia group E protein, is involved in the mediation of both protein localization and DNA repair. Mutation of the gene is associated with Fanconi anemia." @default.
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- NCIT_C86552 NCIT_P100 "613976" @default.
- NCIT_C86552 NCIT_P102 "AF265210" @default.
- NCIT_C86552 NCIT_P106 "Gene or Genome" @default.
- NCIT_C86552 NCIT_P107 "FANCE wt Allele" @default.
- NCIT_C86552 NCIT_P108 "FANCE wt Allele" @default.
- NCIT_C86552 NCIT_P207 "C2828055" @default.
- NCIT_C86552 NCIT_P321 "2178" @default.
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- NCIT_C86552 normalizedInformationContent "100" @default.
- NCIT_C86552 referenceCount "1" @default.
- NCIT_C86552 hasExactSynonym "FA Complementation Group E wt Allele" @default.
- NCIT_C86552 hasExactSynonym "FACE" @default.
- NCIT_C86552 hasExactSynonym "FAE" @default.
- NCIT_C86552 hasExactSynonym "FANCE wt Allele" @default.
- NCIT_C86552 hasExactSynonym "Fanconi Anemia Complementation Group E Gene" @default.
- NCIT_C86552 hasExactSynonym "Fanconi Anemia, Complementation Group E Gene" @default.
- NCIT_C86552 inSubset NCIT_C116977 @default.
- NCIT_C86552 inSubset NCIT_C142799 @default.
- NCIT_C86552 inSubset NCIT_C142800 @default.
- NCIT_C86552 type Class @default.
- NCIT_C86552 isDefinedBy ncit.owl @default.
- NCIT_C86552 label "FANCE wt Allele" @default.
- NCIT_C86552 subClassOf B05e3519229abc1cc31e40cc8feb30da5 @default.
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