Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_provenance.
- NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_assertion wasGeneratedBy ECO_0000203 NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_provenance.
- NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_assertion wasDerivedFrom gad-20150221 NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_provenance.
- NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_assertion SIO_000772 17650440 NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_provenance.
- NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_assertion evidence source_evidence_literature NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_provenance.
- NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_assertion description "[The risk of recurrent venous thromboembolism among heterozygous carriers of factor V Leiden or prothrombin G20210A mutation. A systematic review of prospective studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP109357.RA0e3lrPh6t4A71Lou64Er4Dhoo3WoPJdhHt9ryAiegCQ130_provenance.