Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_provenance.
- NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_assertion description "[While the common APOE polymorphism explains the majority of the locus genetic determinants of plasma lipid levels, additional SNPs in the APOC1/C2 region may contribute to CHD risk, but these effects require confirmation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_provenance.
- NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_assertion evidence source_evidence_literature NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_provenance.
- NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_assertion SIO_000772 20498921 NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_provenance.
- NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_assertion wasDerivedFrom befree-2016 NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_provenance.
- NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_assertion wasGeneratedBy ECO_0000203 NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_provenance.
- befree-2016 importedOn "2016-02-19" NP814348.RAv5BMkwmYbrN3O1VjgUfLnJG_BuEi5u7wonOOFo6Cagg130_provenance.