Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_provenance.
- NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_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." NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_provenance.
- NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_assertion evidence source_evidence_literature NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_provenance.
- NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_assertion SIO_000772 18195193 NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_provenance.
- NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_assertion wasDerivedFrom befree-2016 NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_provenance.
- NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_assertion wasGeneratedBy ECO_0000203 NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_provenance.
- befree-2016 importedOn "2016-02-19" NP649960.RAV3Xk9AR5fnvvAm3evNBSm8g8Ae8oHVdGnExqsT2Lxm0130_provenance.