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- source_evidence_literature type ECO_0000212 NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_provenance.
- NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_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." NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_provenance.
- NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_assertion evidence source_evidence_literature NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_provenance.
- NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_assertion SIO_000772 12732394 NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_provenance.
- NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_assertion wasDerivedFrom befree-20150227 NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_provenance.
- NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_assertion wasGeneratedBy ECO_0000203 NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_provenance.
- befree-20150227 importedOn "2015-02-27" NP531621.RAbFiIjK4dKh360v3C_In11xvIWk4fin_S90cdtx1PIag130_provenance.