Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance.
- NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_assertion description "[Benign familial neonatal convulsion (BFNC) is a rare autosomal dominant disorder caused by mutations in two genes, KCNQ2 and KCNQ3, encoding for potassium channel subunits underlying the M-current.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance.
- NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_assertion evidence source_evidence_literature NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance.
- NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_assertion SIO_000772 15249611 NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance.
- NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_assertion wasDerivedFrom befree-20140225 NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance.
- NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_assertion wasGeneratedBy ECO_0000203 NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance.