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- NCIT_C50987 IAO_0000115 "Human FANCG wild-type allele is located within 9p13 and is approximately 6 kb in length. This allele, which encodes fanconi anemia group G protein, is involved in chromosomal stability and maintenance and DNA interstrand cross-link repair. The allele also plays a putative role in post-replication repair and cell cycle checkpoints. Allelic variants are involved in Fanconi syndrome." @default.
- NCIT_C50987 NCIT_NHC0 "C50987" @default.
- NCIT_C50987 NCIT_P100 "602956" @default.
- NCIT_C50987 NCIT_P102 "NM_004629" @default.
- NCIT_C50987 NCIT_P106 "Gene or Genome" @default.
- NCIT_C50987 NCIT_P107 "FANCG wt Allele" @default.
- NCIT_C50987 NCIT_P108 "FANCG wt Allele" @default.
- NCIT_C50987 NCIT_P207 "C1707999" @default.
- NCIT_C50987 NCIT_P211 "DNA repair" @default.
- NCIT_C50987 NCIT_P211 "cell cycle checkpoint" @default.
- NCIT_C50987 NCIT_P211 "damaged DNA binding" @default.
- NCIT_C50987 NCIT_P211 "regulation of cell cycle" @default.
- NCIT_C50987 NCIT_P321 "2189" @default.
- NCIT_C50987 NCIT_P322 "CTRP" @default.
- NCIT_C50987 NCIT_P366 "FANCG_wt_Allele" @default.
- NCIT_C50987 NCIT_P96 "DNA Repair Protein XRCC9" @default.
- NCIT_C50987 NCIT_R130 NCIT_C20633 @default.
- NCIT_C50987 NCIT_R130 NCIT_C38997 @default.
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- NCIT_C50987 NCIT_R175 NCIT_C80693 @default.
- NCIT_C50987 NCIT_R175 NCIT_C94810 @default.
- NCIT_C50987 NCIT_R37 NCIT_C16513 @default.
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- NCIT_C50987 NCIT_R37 NCIT_C41543 @default.
- NCIT_C50987 NCIT_R40 NCIT_C12219 @default.
- NCIT_C50987 NCIT_R40 NCIT_C13282 @default.
- NCIT_C50987 NCIT_R40 NCIT_C13377 @default.
- NCIT_C50987 NCIT_R40 NCIT_C13432 @default.
- NCIT_C50987 NCIT_R40 NCIT_C13446 @default.
- NCIT_C50987 NCIT_R40 NCIT_C14135 @default.
- NCIT_C50987 NCIT_R40 NCIT_C25125 @default.
- NCIT_C50987 NCIT_R40 NCIT_C32221 @default.
- NCIT_C50987 NCIT_R40 NCIT_C34070 @default.
- NCIT_C50987 NCIT_R41 NCIT_C14182 @default.
- NCIT_C50987 NCIT_R41 NCIT_C14225 @default.
- NCIT_C50987 NCIT_R41 NCIT_C14234 @default.
- NCIT_C50987 NCIT_R41 NCIT_C14250 @default.
- NCIT_C50987 NCIT_R41 NCIT_C14262 @default.
- NCIT_C50987 NCIT_R41 NCIT_C14282 @default.
- NCIT_C50987 NCIT_R41 NCIT_C25796 @default.
- NCIT_C50987 NCIT_R41 NCIT_C79740 @default.
- NCIT_C50987 normalizedInformationContent "100" @default.
- NCIT_C50987 referenceCount "1" @default.
- NCIT_C50987 hasExactSynonym "FA Complementation Group G wt Allele" @default.
- NCIT_C50987 hasExactSynonym "FACG" @default.
- NCIT_C50987 hasExactSynonym "FAG Gene" @default.
- NCIT_C50987 hasExactSynonym "FANCG wt Allele" @default.
- NCIT_C50987 hasExactSynonym "Fanconi Anemia Complementation Group G Gene" @default.
- NCIT_C50987 hasExactSynonym "Fanconi Anemia, Complementation Group G Gene" @default.
- NCIT_C50987 hasExactSynonym "X-Ray Repair Complementing Defective Repair In Chinese Hamster Cells 9 Gene" @default.
- NCIT_C50987 hasExactSynonym "X-Ray Repair, Complementing Defective, In Chinese Hamster, 9 Gene" @default.
- NCIT_C50987 hasExactSynonym "XRCC9 Gene" @default.
- NCIT_C50987 inSubset NCIT_C116977 @default.
- NCIT_C50987 inSubset NCIT_C142799 @default.
- NCIT_C50987 inSubset NCIT_C142800 @default.
- NCIT_C50987 type Class @default.
- NCIT_C50987 isDefinedBy ncit.owl @default.
- NCIT_C50987 label "FANCG wt Allele" @default.
- NCIT_C50987 subClassOf NCIT_C159207 @default.
- NCIT_C50987 subClassOf NCIT_C16612 @default.
- NCIT_C50987 subClassOf NCIT_C18297 @default.
- NCIT_C50987 subClassOf NCIT_C19676 @default.
- NCIT_C50987 subClassOf NCIT_C24385 @default.
- NCIT_C50987 subClassOf NCIT_C50987 @default.
- NCIT_C50987 equivalentClass B847a96e376bdeb2fabae67d09825f6c1 @default.
- NCIT_C50987 equivalentClass Bd648641448b7a8be1a27edf4d29539ac @default.