Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_provenance.
- NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_assertion description "[Polymorphisms of the renin-angiotensin-aldosterone system (RAAS) represent an attractive hypothesis as potential disease modifiers, as these genetic variants alter the 'activation status' of the RAAS, which leads to more left ventricular hypertrophy through different pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_provenance.
- NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_assertion evidence source_evidence_literature NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_provenance.
- NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_assertion SIO_000772 21507890 NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_provenance.
- NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_assertion wasDerivedFrom befree-20150227 NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_provenance.
- NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_assertion wasGeneratedBy ECO_0000203 NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_provenance.
- befree-20150227 importedOn "2015-02-27" NP669840.RAxEBj9aK6KcJpMfbjn2xtfrAyg-4aPz2pNQsclkWu6Os130_provenance.