Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_assertion> ?p ?o ?g. }
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- NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_assertion type Assertion NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_head.
- NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_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." NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_provenance.
- NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_assertion evidence source_evidence_literature NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_provenance.
- NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_assertion SIO_000772 19464834 NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_provenance.
- NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_assertion wasDerivedFrom befree-2016 NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_provenance.
- NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_assertion wasGeneratedBy ECO_0000203 NP740710.RATysLvrq-fJQ7Gs79waqhPhbIu6QHk_786w4pK9DLsF4130_provenance.