Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_provenance.
- NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_assertion description "[In conclusion, LRP gene polymorphisms, particularly the relatively common exon 22 C200T polymorphism, are a significant risk factor for premature CAD in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_provenance.
- NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_assertion evidence source_evidence_literature NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_provenance.
- NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_assertion SIO_000772 12732394 NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_provenance.
- NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_assertion wasDerivedFrom befree-2016 NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_provenance.
- NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_assertion wasGeneratedBy ECO_0000203 NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_provenance.
- befree-2016 importedOn "2016-02-19" NP393344.RAxsLlVI6jy8Thjz7Knz8czqGMs6Ibz-AFDV5Ywt2anw8130_provenance.