Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_provenance.
- NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_assertion description "[Mutations in the neuronal nicotinic acetylcholine receptor alpha4 and beta2 subunit genes have been detected in families with autosomal dominant nocturnal frontal lobe epilepsy, and those of two K(+) channel genes were identified to be responsible for underlying genetic abnormalities of benign familial neonatal convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_provenance.
- NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_assertion evidence source_evidence_literature NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_provenance.
- NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_assertion SIO_000772 12204289 NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_provenance.
- NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_assertion wasDerivedFrom befree-20140225 NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_provenance.
- NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_assertion wasGeneratedBy ECO_0000203 NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP378739.RA1nkm7D-EzMw-odAA_suK_y733pqSWnShgcqYcSsu44Y130_provenance.