Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_provenance.
- NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_assertion description "[Although the USF1 gene has been shown to have a critical role in the etiology of familial combined hyperlipidemia, which predisposes to early CVD, the gene's potential role as a risk factor for CVD events at the population level has not been established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_provenance.
- NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_assertion evidence source_evidence_literature NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_provenance.
- NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_assertion SIO_000772 16699592 NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_provenance.
- NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_assertion wasDerivedFrom befree-20140225 NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_provenance.
- NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_assertion wasGeneratedBy ECO_0000203 NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_provenance.
- befree-20140225 importedOn "2014-02-25" NP227167.RAx2MoFHMmh4hW5qRM0oSlwwy_MgxL_TbTZtaAGvB4L30130_provenance.