Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_provenance.
- NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_assertion description "[Mutations in the chloride channel gene CLCN2 have been associated with the most common forms of idiopathic generalized epilepsies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_provenance.
- NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_assertion evidence source_evidence_literature NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_provenance.
- NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_assertion SIO_000772 15021241 NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_provenance.
- NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_assertion wasDerivedFrom befree-20140225 NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_provenance.
- NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_assertion wasGeneratedBy ECO_0000203 NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP591038.RA31X2THyB5fgNhQbfH6RasXi63E5oY3bwRUHfZgmwtk0130_provenance.