Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance.
- NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_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." NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance.
- NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_assertion evidence source_evidence_literature NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance.
- NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_assertion SIO_000772 21507890 NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance.
- NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_assertion wasDerivedFrom befree-2016 NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance.
- NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_assertion wasGeneratedBy ECO_0000203 NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance.
- befree-2016 importedOn "2016-02-19" NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance.