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- source_evidence_literature type ECO_0000212 NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_provenance.
- NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_assertion description "[Our purpose was to evaluate associations of single nucleotide polymorphisms (SNPs) at the low density lipoprotein (LDL) receptor (LDLR C44857T, minor allele frequency (MAF) 0.26, and A44964G, MAF 0.25, both in the untranslated region) and HMG-CoA reductase (HMGCR i18 T>G, MAF 0.019) gene loci with baseline lipid values, statin-induced LDL-cholesterol (C) lowering response, and incident coronary heart disease (CHD) and cardiovascular disease (CVD) on trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_provenance.
- NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_assertion evidence source_evidence_literature NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_provenance.
- NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_assertion SIO_000772 18261733 NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_provenance.
- NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_assertion wasDerivedFrom befree-2016 NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_provenance.
- NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_assertion wasGeneratedBy ECO_0000203 NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_provenance.
- befree-2016 importedOn "2016-02-19" NP654493.RAvOwvDdO6YIS7-PBm_Onjyr8iu1unjvi1zBN6xxYb1jE130_provenance.