Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_assertion type Assertion NP667278.RARdO9gGmny0Mlx4OblOjT2yhDvAfgx1hcn0p5P5ACgEw130_head.
- 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.