Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_provenance.
- NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_assertion description "[We examined the association between different polymorphisms frequently found in young patients with cryptogenic stroke [methylenetetrahydrofolate reductase (MTHFR) C677T, factor II (prothrombin) G20210A, factor V G1691A (Leiden), nitric oxide synthase 3 (NOS3) intron 4 VNTR, and apolipoprotein E (APOE) epsilon4 gene] in patients with a cerebral infarct caused by spontaneous cervical artery dissection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_provenance.
- NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_assertion evidence source_evidence_literature NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_provenance.
- NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_assertion SIO_000772 20446941 NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_provenance.
- NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_assertion wasDerivedFrom befree-20140225 NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_provenance.
- NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_assertion wasGeneratedBy ECO_0000203 NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP881011.RAQjC3576S2PfFaRk1xDcO3RPGWgYs-kF0FEhK0sgmj9k130_provenance.