Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_provenance.
- NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_assertion description "[Our study provides mixed evidence that variation in PCSK9 may contribute to genetic risk of PAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_provenance.
- NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_assertion evidence source_evidence_literature NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_provenance.
- NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_assertion SIO_000772 18436227 NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_provenance.
- NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_assertion wasDerivedFrom gad-20130706 NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_provenance.
- NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_assertion wasGeneratedBy ECO_0000203 NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP77647.RACeVR2In73qzPHw71s81v1iBrdSraCuqUxlQoJglm2UI130_provenance.