Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_provenance.
- NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_assertion description "[The association was confirmed in an independent CAD case-control sample (CATHGEN) and strong association with MI was identified with single nucleotide polymorphisms (SNPs) in the 3' end of FAM5C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_provenance.
- NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_assertion evidence source_evidence_literature NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_provenance.
- NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_assertion SIO_000772 18430236 NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_provenance.
- NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_assertion wasDerivedFrom befree-2016 NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_provenance.
- NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_assertion wasGeneratedBy ECO_0000203 NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_provenance.
- befree-2016 importedOn "2016-02-19" NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_provenance.