Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• NP264465.RAbjLVQay2ndT6S_sDaf9dP2RvjOLnT3H5_FnmTtAqdcU130_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." NP264465.RAbjLVQay2ndT6S_sDaf9dP2RvjOLnT3H5_FnmTtAqdcU130_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.
• NP614717.RASmNJsIzfo27UthLE4B3nGK-PIEEpMW6FXPGUBaEcHOk130_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." NP614717.RASmNJsIzfo27UthLE4B3nGK-PIEEpMW6FXPGUBaEcHOk130_provenance.
• NP348606.RA99pUaxD4HhL3AWZAEu79ILOoxHxt9rHNg_8qMwcOfGY130_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." NP348606.RA99pUaxD4HhL3AWZAEu79ILOoxHxt9rHNg_8qMwcOfGY130_provenance.
• NP395063.RA-Zvs69HZV6S7oOJCVx-zJ4YyN_PlsuwnVussgWIDjMg130_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." NP395063.RA-Zvs69HZV6S7oOJCVx-zJ4YyN_PlsuwnVussgWIDjMg130_provenance.
• NP332287.RAkOEOH1Xx7eiELup6t9hKKZ3IJJYHK7z4LQorS4FuxME130_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." NP332287.RAkOEOH1Xx7eiELup6t9hKKZ3IJJYHK7z4LQorS4FuxME130_provenance.
• NP393140.RAuQiLNACtHvbCCc7V0cA7_6u-lyVtSs1xpBA_aLW53d0130_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." NP393140.RAuQiLNACtHvbCCc7V0cA7_6u-lyVtSs1xpBA_aLW53d0130_provenance.
• NP387785.RAeICd33BN5VGoupIFsYlaiWDVUMpdsD3yxa9OCMBwva8130_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." NP387785.RAeICd33BN5VGoupIFsYlaiWDVUMpdsD3yxa9OCMBwva8130_provenance.
• 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.
• NP458021.RAlVZzCV-OGidV5JnqA3NNuZj7FOBp7FqiwA1Mo_PV-hc130_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." NP458021.RAlVZzCV-OGidV5JnqA3NNuZj7FOBp7FqiwA1Mo_PV-hc130_provenance.
• NP754443.RAmnOUYANG00wdIGQM_bTAVAfbWYFMYYiGRlxRZkBhTbc130_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." NP754443.RAmnOUYANG00wdIGQM_bTAVAfbWYFMYYiGRlxRZkBhTbc130_provenance.
• NP584814.RA_nszuqNKTC4Wu1U25AXo49BlNBY1BEF51JLIGj1Lmg8130_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." NP584814.RA_nszuqNKTC4Wu1U25AXo49BlNBY1BEF51JLIGj1Lmg8130_provenance.
• NP523387.RAfsHtrNdcFys744eN4uW9qValkvvHasG5eHDtq4VKGKw130_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." NP523387.RAfsHtrNdcFys744eN4uW9qValkvvHasG5eHDtq4VKGKw130_provenance.
• 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." provenance.
• 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." provenance.
• NP740708.RACo1i9KQYwEHjBJbt4CMlltjUKkV1Ek0FHPYdCWAPLj8130_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." NP740708.RACo1i9KQYwEHjBJbt4CMlltjUKkV1Ek0FHPYdCWAPLj8130_provenance.
• NP740711.RABsN3b9b6mP2L8AVZSNAsIGx__UcpHUsF72_XIhAdohU130_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." NP740711.RABsN3b9b6mP2L8AVZSNAsIGx__UcpHUsF72_XIhAdohU130_provenance.
• 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.
• NP740713.RAcDB5bk_eIvqPu9lMEWbF4oZg0Frp3my4awFIvuYFqfQ130_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." NP740713.RAcDB5bk_eIvqPu9lMEWbF4oZg0Frp3my4awFIvuYFqfQ130_provenance.
• NP740706.RAvdb2piHq-tdR6imCm01pmF7yRip3jnlLaqg1NfjWwfA130_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." NP740706.RAvdb2piHq-tdR6imCm01pmF7yRip3jnlLaqg1NfjWwfA130_provenance.
• NP740707.RAun_4Q5gaYG-ndWKvEBHVipIb8dg9ETgPsvhiibd9g70130_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." NP740707.RAun_4Q5gaYG-ndWKvEBHVipIb8dg9ETgPsvhiibd9g70130_provenance.
• NP523456.RAPdDvmQmIpI1wDPw09YUF-nwpdTCaJRwRa5N66wFuu_4130_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." NP523456.RAPdDvmQmIpI1wDPw09YUF-nwpdTCaJRwRa5N66wFuu_4130_provenance.
• NP523476.RAI-sis6ybZvhnYhP3e2ut4YbgmY07AaLC_UQklbdPzCo130_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." NP523476.RAI-sis6ybZvhnYhP3e2ut4YbgmY07AaLC_UQklbdPzCo130_provenance.
• NP523353.RAzxPOh_EcfdS0DakytsSLuMraWpmvOBhheYXfOxMctiY130_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." NP523353.RAzxPOh_EcfdS0DakytsSLuMraWpmvOBhheYXfOxMctiY130_provenance.
• NP682466.RAIKHKNwKFhYerjv5giXKUf3UT6ovohYdD03L6UZaJvxs130_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." NP682466.RAIKHKNwKFhYerjv5giXKUf3UT6ovohYdD03L6UZaJvxs130_provenance.