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- NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_assertion type Assertion NP890937.RAKI7_ucJ9GmUOx6BV-BJeGlTNhwnv4ngZOaoZmtkgJyY130_head.
- 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.