Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_provenance.
- NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_assertion description "[This study shows that genetic variation of the AGT (M235T), but not the ACE (I/D), genotypes contributes to the presence of CHD independently of blood pressure profile in a subset of the Spanish population with a high prevalence of cardiovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_provenance.
- NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_assertion evidence source_evidence_literature NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_provenance.
- NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_assertion SIO_000772 11345362 NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_provenance.
- NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_assertion wasDerivedFrom gad-20130706 NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_provenance.
- NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_assertion wasGeneratedBy ECO_0000203 NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_provenance.
- gad-20130706 importedOn "2013-07-06" NP48878.RAyz7DpLi7U0zVF5Vq6VW_ed9176V-zhQA4Gb3CnJsuEY130_provenance.