Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_provenance.
- NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_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." NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_provenance.
- NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_assertion evidence source_evidence_literature NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_provenance.
- NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_assertion SIO_000772 20446941 NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_provenance.
- NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_assertion wasDerivedFrom befree-20140225 NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_provenance.
- NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_assertion wasGeneratedBy ECO_0000203 NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP183250.RARqOtW0vSJ2QUTcExj6wGrpMTsRaNEpuXv4bym2ESDIo130_provenance.