Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_provenance.
- NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_assertion description "[In individual single nucleotide polymorphism analysis, after adjustment for multiple comparisons, a significantly decreased RCC risk was observed for the heterozygous genotype of XPD Asp312Asn [odds ratio (OR) = 0.62; 95% confidence interval (CI): 0.43-0.90] and for the heterozygous and homozygous variant genotypes combined in a dominant model (OR = 0.64; 95% CI: 0.46-0.89).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_provenance.
- NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_assertion evidence source_evidence_literature NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_provenance.
- NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_assertion SIO_000772 18711149 NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_provenance.
- NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_assertion wasDerivedFrom befree-20140225 NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_provenance.
- NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_assertion wasGeneratedBy ECO_0000203 NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP777153.RAKXIYQIlnYyPv5X_ybRj_z4xdCrYTm_he12tTUoxC_zY130_provenance.