Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_assertion> ?p ?o ?g. }
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- NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_assertion type Assertion NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_head.
- NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_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." NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_provenance.
- NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_assertion evidence source_evidence_literature NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_provenance.
- NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_assertion SIO_000772 19464834 NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_provenance.
- NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_assertion wasDerivedFrom befree-20140225 NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_provenance.
- NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_assertion wasGeneratedBy ECO_0000203 NP934780.RAfiLHs-wg7MA6oPvkvB7AtjwXbK8OEc0e1rU7kdA77VQ130_provenance.