Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_provenance.
- NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_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 of increased susceptibility to COPD in the Slovak population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_provenance.
- NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_assertion evidence source_evidence_literature NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_provenance.
- NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_assertion SIO_000772 18461673 NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_provenance.
- NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_assertion wasDerivedFrom gad-20150221 NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_provenance.
- NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_assertion wasGeneratedBy ECO_0000203 NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP50931.RArss2X3UAdwlYbt9QN7e3vcXABTLx9Tk2_hYNoRfIdA4130_provenance.