Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_provenance.
- NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_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." NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_provenance.
- NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_assertion evidence source_evidence_literature NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_provenance.
- NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_assertion SIO_000772 18461673 NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_provenance.
- NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_assertion wasDerivedFrom befree-20150227 NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_provenance.
- NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_assertion wasGeneratedBy ECO_0000203 NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP437763.RAO1ZwmKQp1u4VjjY36P0qJMgSYNiWQKtCjS2rC7-9M0I130_provenance.