Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_provenance.
- NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_assertion description "[In conclusion, LRP gene polymorphisms, particularly the relatively common exon 22 C200T polymorphism, are a significant risk factor for premature CAD in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_provenance.
- NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_assertion evidence source_evidence_literature NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_provenance.
- NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_assertion SIO_000772 12732394 NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_provenance.
- NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_assertion wasDerivedFrom befree-20140225 NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_provenance.
- NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_assertion wasGeneratedBy ECO_0000203 NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_provenance.