Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_provenance.
- NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_assertion description "[The role of common APOE variants on plasma lipids, particularly low density lipoprotein (LDL) levels, and coronary heart disease (CHD) risk is well known; the influence of variation in the other nearby apolipoprotein genes APOC1, APOC4 and APOC2 is unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_provenance.
- NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_assertion evidence source_evidence_literature NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_provenance.
- NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_assertion SIO_000772 20498921 NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_provenance.
- NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_assertion wasDerivedFrom gad-20150221 NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_provenance.
- NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_assertion wasGeneratedBy ECO_0000203 NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP177012.RAzL6mwIk7JrKEmNNsNOx5M0_lE6AuVQYJ26cGmDyLPAs130_provenance.