Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_provenance.
- befree-2016 importedOn "2016-02-19" NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_provenance.
- NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_assertion wasGeneratedBy ECO_0000203 NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_provenance.
- NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_assertion wasDerivedFrom befree-2016 NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_provenance.
- NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_assertion SIO_000772 10351920 NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_provenance.
- NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_assertion evidence source_evidence_literature NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_provenance.
- NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_assertion description "[Several polymorphisms of genes encoding for components of the renin angiotensin system such as the M235T polymorphism in the angiotensinogen gene, the 287-base-pair insertion (I)/deletion (D) polymorphism at intron 16 of the ACE gene, and the A1166C polymorphism in the angiotensin II type 1 receptor gene have been associated with an increased risk of cardiovascular diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253757.RA7DPyGotkNnFkV5FV4F_Xthx95Q4YbS6cwbz44Vc4WpE130_provenance.