Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance.
- NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_assertion description "[Although none of the tested gene polymorphisms was significantly related to an increased risk of COPD alone, our results suggest that the homozygous exon 3 mutant variant of EPHX1 gene in the combination with GSTM1 null genotype is a significant predictor]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance.
- NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_assertion evidence source_evidence_literature NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance.
- NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_assertion SIO_000772 18461673 NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance.
- NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_assertion wasDerivedFrom gad-20150221 NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance.
- NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_assertion wasGeneratedBy ECO_0000203 NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance.