Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_provenance.
- NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_assertion description "[The CYP1A1*2C (p = 0.011, OR: 6.62, and 95% CI: 1.56-28.10), GSTT1 null (p < or = 0.001, OR: 11.94, 95% CI: 7.88-18.12), and GSTP1 TT genotypes (p = 0.017, OR: 3.42, 95% CI 1.26-9.38) demonstrated significant association of DLBCL risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_provenance.
- NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_assertion evidence source_evidence_literature NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_provenance.
- NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_assertion SIO_000772 18203021 NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_provenance.
- NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_assertion wasDerivedFrom befree-20150227 NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_provenance.
- NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_assertion wasGeneratedBy ECO_0000203 NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP440584.RAPJxlRhFExW0mbf-eoabOlNl1zh7XuOU3Oh2lFqVf1KA130_provenance.