Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_provenance.
- NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_assertion description "[Persons homozygous for haplotype 3, which is a common variant of the glucocorticoid receptor gene, had a more than 2-fold increased risk of myocardial infarction (hazard ratio, 2.1; 95% confidence interval, 1.13-4.07) and an almost 3-fold increased risk of coronary heart disease (hazard ratio, 2.6; 95% confidence interval, 1.40-4.81) compared with nonhomozygous persons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_provenance.
- NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_assertion evidence source_evidence_literature NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_provenance.
- NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_assertion SIO_000772 18195193 NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_provenance.
- NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_assertion wasDerivedFrom befree-20150227 NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_provenance.
- NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_assertion wasGeneratedBy ECO_0000203 NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434807.RAR-oH48LHJBHD-GYPs8i1qDZq4gaiKmmeQoz_xRaT15o130_provenance.