Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_provenance.
- NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_assertion description "[Our results indicate that SNPs in the NER genes ERCC1 (Asn118Asn, 15310G>C, 8902G>T), XPA (-4G>A), ERCC2/XPD (Lys751Gln) and ERCC5/XPD (His46His); the BER genes APE1/APEX (Ile64Val), OGG1 (Ser326Cys), PCNA (1876A>G) and XRCC1 (Arg194Trp, Arg280His, Arg399Gln); and the DSB-R genes ATR (Thr211Met), NBS1 (Glu185Gln), XRCC2 (Arg188His) and XRCC9 (Thr297Ile) modulate NSCLC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_provenance.
- NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_assertion evidence source_evidence_literature NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_provenance.
- NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_assertion SIO_000772 16195237 NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_provenance.
- NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_assertion wasDerivedFrom befree-20140225 NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_provenance.
- NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_assertion wasGeneratedBy ECO_0000203 NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP361625.RASNAGn-5bxgBTDgigSDD4k5zCbaN7f_qxFqEFTvF6iw8130_provenance.