Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_provenance.
- NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_assertion description "[We assessed the frequencies of factor V Leiden and prothrombin variant G20210A to determine whether particular inherited haemostatic risk factors may have contribution to the development of prothrombotic state in atrial fibrillation patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_provenance.
- NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_assertion evidence source_evidence_literature NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_provenance.
- NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_assertion SIO_000772 15087601 NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_provenance.
- NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_assertion wasDerivedFrom befree-20150227 NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_provenance.
- NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_assertion wasGeneratedBy ECO_0000203 NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP389649.RAu20Nsjh7yv-uVymwv55atu4KXiT6GWhhldlxa0ZLtZc130_provenance.