Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_provenance.
- NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_assertion description "[We found a significantly higher frequency of SNP rs4819554 AA homozygotes among individuals with eGFR<60 ml/min/1.73 m(2) (n=90) (p=0.005, OR=2.11; 1.26-3.54), an effect that was independent of the presence of type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_provenance.
- NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_assertion evidence source_evidence_literature NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_provenance.
- NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_assertion SIO_000772 25636567 NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_provenance.
- NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_assertion wasDerivedFrom befree-2016 NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_provenance.
- NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_assertion wasGeneratedBy ECO_0000203 NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1259650.RAW7bIGetw3l9izQvwx-kRzBaakhq-Uhk-xN4I1uQ3lpk130_provenance.