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- source_evidence_literature type ECO_0000212 NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_provenance.
- NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_assertion description "[Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), nucleotide excision repair (XPC-PAT, XPA-23G>A, ERCC1-19007T>C and XPD-L751Q), recombination (XRCC3-T241M) and alkylation damage reversal (MGMT-L84F) were tested for their potential role in the development of GC by using logistic regression models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_provenance.
- NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_assertion evidence source_evidence_literature NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_provenance.
- NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_assertion SIO_000772 20817763 NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_provenance.
- NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_assertion wasDerivedFrom befree-2016 NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_provenance.
- NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_assertion wasGeneratedBy ECO_0000203 NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_provenance.
- befree-2016 importedOn "2016-02-19" NP837196.RA_Lqpin-FWN1Iz7EhEbJp6P9IawpuJPWFPReceitpqn4130_provenance.