Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_assertion> ?p ?o ?g. }
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- NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_assertion type Assertion NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_head.
- NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_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." NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_provenance.
- NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_assertion evidence source_evidence_literature NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_provenance.
- NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_assertion SIO_000772 12732394 NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_provenance.
- NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_assertion wasDerivedFrom befree-20140225 NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_provenance.
- NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_assertion wasGeneratedBy ECO_0000203 NP246254.RAnUZHAFOR-rkMS6VFi29smjCnoShid2MvFDEiTXy0Sd4130_provenance.