Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489184.RAl6BcfJW3rH5IPd71zJ74Db9YWk3JNScz9fyLKaCaXtQ130_provenance.
• NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_provenance.
• NP927569.RAeucBA_WVI37gEGAysxR4QkUJgecJNNiB58GIOr4PdGs130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927569.RAeucBA_WVI37gEGAysxR4QkUJgecJNNiB58GIOr4PdGs130_provenance.
• NP552964.RAnTbBbEcyHnbyD1X0jxiQUlYOVBRi-a-wFJnTllISPhM130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552964.RAnTbBbEcyHnbyD1X0jxiQUlYOVBRi-a-wFJnTllISPhM130_provenance.
• assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP188143.RA436j26GORu8DnMPUaeIo-Szgb0a0QftVORC9J6iS__4130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188143.RA436j26GORu8DnMPUaeIo-Szgb0a0QftVORC9J6iS__4130_provenance.
• NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_provenance.
• assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_provenance.
• NP757857.RAwCAbt8XVrR5pQ7QSMlBDKPW20cd05HPHWA2raex3l60130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP757857.RAwCAbt8XVrR5pQ7QSMlBDKPW20cd05HPHWA2raex3l60130_provenance.
• NP523555.RATf7AcO9FDw0vSQjUYxAyBxWZZRnBjnhK_unsyVKlFMg130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523555.RATf7AcO9FDw0vSQjUYxAyBxWZZRnBjnhK_unsyVKlFMg130_provenance.
• NP523559.RAf6aZ-4S5YD0r8ifLWj_ko8eDfW6r0qsMeP3uLUENmWU130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523559.RAf6aZ-4S5YD0r8ifLWj_ko8eDfW6r0qsMeP3uLUENmWU130_provenance.
• assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP417024.RAk8vrAWaJnH75yvwU_G-9XGsxxbu1HrvSyyOxmzUCJKY130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417024.RAk8vrAWaJnH75yvwU_G-9XGsxxbu1HrvSyyOxmzUCJKY130_provenance.
• NP523551.RAoU7O1bHkdBbXS9zGcdD1O5Q0uRE7wtJkEp2TxCSRyJY130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523551.RAoU7O1bHkdBbXS9zGcdD1O5Q0uRE7wtJkEp2TxCSRyJY130_provenance.
• NP417127.RAxDjOXL4sfLcJ5HqoPwcP_YymKg-_L4usSDFn1o75IhU130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417127.RAxDjOXL4sfLcJ5HqoPwcP_YymKg-_L4usSDFn1o75IhU130_provenance.
• NP416978.RA-2f4QXdWhZrd0SRhYGATUHBbA70dWoJiRAHRiu8q2_g130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416978.RA-2f4QXdWhZrd0SRhYGATUHBbA70dWoJiRAHRiu8q2_g130_provenance.
• NP523552.RAOLqF1fMa7MRSxAPG3xBwADM-mKKia5rpdt7Db69zg2w130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523552.RAOLqF1fMa7MRSxAPG3xBwADM-mKKia5rpdt7Db69zg2w130_provenance.
• NP523558.RAMw9sUE2rEF7T4-rvPziiieqfAYNfEzEK_HI0_bdq1Mg130_assertion description "[Mutations in GABRA1, GABRG2, and GABRB3 are associated with absence seizures, while mutations in CLCN2 and myoclonin/EFHC1 substantiate juvenile myoclonic epilepsy as a clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523558.RAMw9sUE2rEF7T4-rvPziiieqfAYNfEzEK_HI0_bdq1Mg130_provenance.