Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_provenance.
- NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_assertion description "[None of the SNPs on these loci independently could modify the risk of the diseases in overall population but variant genotype (Gln/Gln) at codon 399 on XRCC1 and major genotype (Lys/Lys) at codon 751 on XPD were associated with increased risk of leukoplakia and cancer among slow acetylators, respectively (OR = 4.2, 95% CI = 1.2-15.0; OR = 1.6, 95% CI = 1.1-2.3, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_provenance.
- NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_assertion evidence source_evidence_literature NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_provenance.
- NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_assertion SIO_000772 17290401 NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_provenance.
- NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_assertion wasDerivedFrom befree-20150227 NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_provenance.
- NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_assertion wasGeneratedBy ECO_0000203 NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP381873.RAKNVIDp8tJldmwcob0F9FejXwQ9xIbSHZ79wt9B4o9Wg130_provenance.