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Matches in Nanopublications for { ?s ?p "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP523463.RAYtkv2DzV8StWGVmH2ps6dqeB5yj2y6c6VlztefdiKqE130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523463.RAYtkv2DzV8StWGVmH2ps6dqeB5yj2y6c6VlztefdiKqE130_provenance.
• assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP276306.RAA4SLa_0PgYtyk-LDQTzI-DsprGtp7xwLAIOrPhch1Do130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276306.RAA4SLa_0PgYtyk-LDQTzI-DsprGtp7xwLAIOrPhch1Do130_provenance.
• NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523381.RAgJpnqpxxoXfwpeZpSyCeb0-5ivOibz8zB-NYDbjIhjg130_provenance.
• NP276307.RAcJShrOXc2A1dngF0Z_PLOsamxraE5nn9x2dYZXWTu_4130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276307.RAcJShrOXc2A1dngF0Z_PLOsamxraE5nn9x2dYZXWTu_4130_provenance.
• NP276308.RAWZsR0xdBaj6elxaG57f7_p10vmZfsdde4wnkwXYI098130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276308.RAWZsR0xdBaj6elxaG57f7_p10vmZfsdde4wnkwXYI098130_provenance.
• NP276310.RATURGPMgkTztf6ZDQOWApVUhPS7hrcW9W2Unrnsv7ziw130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276310.RATURGPMgkTztf6ZDQOWApVUhPS7hrcW9W2Unrnsv7ziw130_provenance.
• NP333894.RAt-X0Ia45kbaP9dbQFJ2qa7X5BRf7seyWkxydKScSEJ0130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333894.RAt-X0Ia45kbaP9dbQFJ2qa7X5BRf7seyWkxydKScSEJ0130_provenance.
• NP314282.RA4ajDCS9gr-_S6uL8KLkQGfCXni_tRp17RZrt9v7mJUM130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314282.RA4ajDCS9gr-_S6uL8KLkQGfCXni_tRp17RZrt9v7mJUM130_provenance.
• NP523470.RAx3ldqlJFOMiDak5Iiadn-h8Sd5prKeylpgxloK5IYrY130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523470.RAx3ldqlJFOMiDak5Iiadn-h8Sd5prKeylpgxloK5IYrY130_provenance.
• NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_assertion description "[Microsatellite markers linked to juvenile myoclonic epilepsy (EJM1), benign neonatal familial convulsions EBN1 and EBN2, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), idiopathic generalized epilepsy (EGI), progressive myoclonic epilepsy of Unverricht-Lundborg (EPM1), and partial epilepsy with auditory features (EPT), were also excluded as potential loci linked to the FC trait in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276309.RA_KPvxmoa2dyzGicd9ghmnIbz3pPWI6n3DhDKYf7Q7s4130_provenance.