Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_assertion> ?p ?o ?g. }
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- NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_assertion type Assertion NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_head.
- NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_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." NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_provenance.
- NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_assertion evidence source_evidence_literature NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_provenance.
- NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_assertion SIO_000772 12732394 NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_provenance.
- NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_assertion wasDerivedFrom befree-20140225 NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_provenance.
- NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_assertion wasGeneratedBy ECO_0000203 NP751880.RA9Ka-q6rlnvIfboDrpwlyxYvYLo7cpCWK9QhvgF4va-I130_provenance.