Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_provenance.
- NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_assertion description "[We examined the association between 36 genotyped and 193 imputed SNPs within four lipid-lowering drug target genes (HMGCR, PPARA, HM74A/GPR109A and CETP) and four non-lipid drug target genes (ACE, AGTR1, P2RY12, and ATP4B) and lipid phenotypes, blood pressure, and coronary artery disease in 5635 adult participants of the Lausanne, Switzerland, CoLaus study, genotyped using the Affymetrix 500K SNP chip technology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_provenance.
- NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_assertion evidence source_evidence_literature NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_provenance.
- NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_assertion SIO_000772 18787507 NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_provenance.
- NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_assertion wasDerivedFrom befree-20150227 NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_provenance.
- NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_assertion wasGeneratedBy ECO_0000203 NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_provenance.
- befree-20150227 importedOn "2015-02-27" NP636328.RAYtVda57b2ePK19uvaaV29-j1LMOEiwsFdo8HHd7Z690130_provenance.