Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_provenance.
- NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_assertion wasGeneratedBy ECO_0000203 NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_provenance.
- NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_assertion wasDerivedFrom befree-20150227 NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_provenance.
- NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_assertion SIO_000772 20966899 NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_provenance.
- NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_assertion evidence source_evidence_literature NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_provenance.
- NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_assertion description "[A silent polymorphism (+1166 A/C single-nucleotide polymorphism) localized in the 3'-UTR (untranslated region) of the human angiotensin II type-1 receptor (AT1R) has been associated with hypertension and cardiovascular complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791666.RAxePSIheaHJpvs8XRd2omXf2r2m3bL3VUEwbi1hffcpk130_provenance.