Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_provenance.
- NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_assertion description "[We found that the null GSTM1 and GSTT1 genotypes were associated with an increase in the risk of developing coronary heart disease (OR = 1.14; 95% CI: 0.71 - 1.82; OR = 1.38; 95% CI: 0.82 - 2.32), respectively, but this increase was not significant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_provenance.
- NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_assertion evidence source_evidence_literature NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_provenance.
- NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_assertion SIO_000772 15088107 NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_provenance.
- NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_assertion wasDerivedFrom befree-20140225 NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_provenance.
- NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_assertion wasGeneratedBy ECO_0000203 NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP592027.RA3RmO_QVJwy5p84FnAbvnEilOwaoOQxKWSQ3OgSSkn_M130_provenance.