Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_assertion> ?p ?o ?g. }
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- NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_assertion type Assertion NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_head.
- 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.