Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_provenance.
- NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_assertion description "[Either the FVL or prothrombin variant was found in 10% (95% confidence interval, 3%-22%) of patients with idiopathic PE compared with 13% (8%-20%) of nonidiopathic PE, 2% (5%-14%) of PE excluded, and 9% (5%-14%) of PE not suspected patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_provenance.
- NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_assertion evidence source_evidence_literature NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_provenance.
- NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_assertion SIO_000772 16574759 NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_provenance.
- NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_assertion wasDerivedFrom befree-20140225 NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_provenance.
- NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_assertion wasGeneratedBy ECO_0000203 NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP554871.RAZeOpeYm4VX6FTqkPrTgkM3QrE-KRt_DBSsJDicFaCW4130_provenance.