Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_provenance.
- befree-2016 importedOn "2016-02-19" NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_provenance.
- NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_assertion wasGeneratedBy ECO_0000203 NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_provenance.
- NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_assertion wasDerivedFrom befree-2016 NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_provenance.
- NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_assertion SIO_000772 12887446 NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_provenance.
- NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_assertion evidence source_evidence_literature NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_provenance.
- NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_assertion description "[Evidence for S284L mutation of the CHRNA4 in a white family with autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403632.RAhr5DI0ew0WABphEPuIyXmdrqLL-U72kDXoMlFWaWLK0130_provenance.