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- NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_assertion type Assertion NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_head.
- NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_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." NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_provenance.
- NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_assertion evidence source_evidence_literature NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_provenance.
- NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_assertion SIO_000772 12732394 NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_provenance.
- NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_assertion wasDerivedFrom befree-2016 NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_provenance.
- NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_assertion wasGeneratedBy ECO_0000203 NP393343.RA3dS7EU-C3mdhk4RC7818nPPnQa3iUTdRxEcivXhVUB0130_provenance.