Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_provenance.
- NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_assertion description "[This study examined the utility of HDL-associated single nucleotide polymorphisms (SNPs) for CVD risk prediction in European Americans with T2D enrolled in the Diabetes Heart Study (DHS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_provenance.
- NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_assertion evidence source_evidence_literature NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_provenance.
- NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_assertion SIO_000772 23799899 NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_provenance.
- NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_assertion wasDerivedFrom befree-20140225 NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_provenance.
- NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_assertion wasGeneratedBy ECO_0000203 NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP567782.RAH6J1mnCoZV-bE5P-zpyMoOdeTFH0nPM0R6YhZp6hFX0130_provenance.