Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_provenance.
- NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_assertion description "[Our best-fitting model showed significant and independent effects of the PI1-deficient allele (odds ratio [OR], 2.0; 95% confidence interval [CI], 1.4 to 3.0) and the ELA2 T-G haplotype (OR, 4.1; 95% CI, 1.9 to 8.9) on lung cancer risk, and an increased risk (OR, 2.6; 95% CI, 2.4 to 2.8) for individuals carrying both a PI1-deficient allele and a G-G haplotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_provenance.
- NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_assertion evidence source_evidence_literature NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_provenance.
- NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_assertion SIO_000772 16002971 NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_provenance.
- NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_assertion wasDerivedFrom befree-20150227 NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_provenance.
- NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_assertion wasGeneratedBy ECO_0000203 NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP989705.RAcj20pg1VRuGRJFkOC_lPqZmOj2E3FAgpEoT6pv6njfc130_provenance.