Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_provenance.
- NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_assertion description "[In this study, CYP1A1 (Ile462Val), CYP1B1(Asn453Ser), GST M1, GSTP1 exon 5�(Ile105Val) and exon 6(Ala114Val) and GSTT1 polymorphisms were determined in 138 patients with advanced NSCLC to evaluate their role in survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_provenance.
- NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_assertion evidence source_evidence_literature NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_provenance.
- NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_assertion SIO_000772 20845989 NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_provenance.
- NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_assertion wasDerivedFrom befree-20140225 NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_provenance.
- NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_assertion wasGeneratedBy ECO_0000203 NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP918029.RA3XwRfNYTAJa4SIKpqFoPYh78usq1A2eM8XNXRQ_UhE0130_provenance.