Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_provenance.
- NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_assertion description "[It has been suggested that the homomer-forming ?7 subunit (CHRNA7) of the neuronal nicotinic acetylcholine receptor (nAChR) is involved in the pathogenesis of common idiopathic generalized epilepsies (IGEs), whereas mutations of the gene coding for the ?4 nAChR subunit (CHRNA4) are associated with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_provenance.
- NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_assertion evidence source_evidence_literature NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_provenance.
- NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_assertion SIO_000772 23553139 NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_provenance.
- NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_assertion wasDerivedFrom befree-20140225 NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_provenance.
- NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_assertion wasGeneratedBy ECO_0000203 NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP339973.RAGB-hWsRNYFaF2WTsYN0JBstxDvRoSik9IxGXry0oxtE130_provenance.