Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_provenance.
- NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_assertion description "[Mutations in the SCN1A gene are found in up to 80% of individuals with severe myoclonic epilepsy of infancy (SMEI), and mutations in KCNQ2 and KCNQ3 were identified in benign familial neonatal convulsions (BFNC) as well as in single families with Rolandic epilepsy (RE) and idiopathic generalized epilepsies (IGE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_provenance.
- NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_assertion evidence source_evidence_literature NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_provenance.
- NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_assertion SIO_000772 19464834 NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_provenance.
- NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_assertion wasDerivedFrom befree-20140225 NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_provenance.
- NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_assertion wasGeneratedBy ECO_0000203 NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP578698.RAfUouNJm67N6RwwDrqRkubVwCfRfWg5E0VSK1sG8aRSs130_provenance.