Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_provenance.
- NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_assertion description "[Our previous study of a Chinese population found the GSTM1 null genotype to be associated with an increased risk of lung AC, and the combination of GSTM1 null genotype and CYP2E1 wild type conferred a significantly elevated risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_provenance.
- NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_assertion evidence source_evidence_literature NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_provenance.
- NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_assertion SIO_000772 14607333 NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_provenance.
- NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_assertion wasDerivedFrom befree-20140225 NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_provenance.
- NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_assertion wasGeneratedBy ECO_0000203 NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_provenance.
- befree-20140225 importedOn "2014-02-25" NP429408.RAvNwOlrNxm8wbhApXfy5zrDiqBmmm5mrIx89hYlK1Iio130_provenance.