Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_provenance.
- NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_assertion description "[Genetic variation at the AGT gene influences the risk of nephropathy in T2DM patients but not extent of DN severity, and thus represents a potential DN genetic susceptibility locus worthy of replication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_provenance.
- NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_assertion evidence source_evidence_literature NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_provenance.
- NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_assertion SIO_000772 21421655 NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_provenance.
- NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_assertion wasDerivedFrom befree-20140225 NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_provenance.
- NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_assertion wasGeneratedBy ECO_0000203 NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP917542.RA3WPEqvVoTMoYoB4Ow6e91zcOmO5Umd1KVGnJOsFpm1U130_provenance.