Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_provenance.
• NP157192.RA5wJo8pYsLjge2SK2hddPGJfPhY299891GQt4pL-vau8130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP157192.RA5wJo8pYsLjge2SK2hddPGJfPhY299891GQt4pL-vau8130_provenance.
• NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP910203.RAsBGAC3e98ywqd6VhfnxrQab2zPyTuVhVOQfnOSrQUkI130_provenance.
• NP775751.RAXGzKsYMmmO7a0KTYsShgqDwcxuT1cYyC5NpSgFL6ZmE130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775751.RAXGzKsYMmmO7a0KTYsShgqDwcxuT1cYyC5NpSgFL6ZmE130_provenance.
• NP496036.RANPIscbLBorMKDG4r1XEMZPLXdBzXwJlepmXEG4QHcEE130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496036.RANPIscbLBorMKDG4r1XEMZPLXdBzXwJlepmXEG4QHcEE130_provenance.
• assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP837856.RAKoewRewVlsS6TOogRTHVpZmGGgIycCxchRdppxmErRo130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837856.RAKoewRewVlsS6TOogRTHVpZmGGgIycCxchRdppxmErRo130_provenance.
• NP682473.RArQt1aAjNzc5BWe51-7vKYi2puep3JehmNVJMOOX4uoQ130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682473.RArQt1aAjNzc5BWe51-7vKYi2puep3JehmNVJMOOX4uoQ130_provenance.
• NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance.
• NP775748.RAMDhGL2VLzG4nrrbldunxkTxUuxKSQuuyM-v2fLRu-qQ130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775748.RAMDhGL2VLzG4nrrbldunxkTxUuxKSQuuyM-v2fLRu-qQ130_provenance.
• NP1054798.RAJTeM1B_moM1PSxnYGdDwZYnVySwRVwCMzt32IrMhlnw130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1054798.RAJTeM1B_moM1PSxnYGdDwZYnVySwRVwCMzt32IrMhlnw130_provenance.
• NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1054801.RAIPgdaTO8pv-xACTLopPBnf-_5FqVbg4F0sCrhbQVOFw130_provenance.
• NP1054799.RA6BqmSLYDDuezkp0WRFMXx1FKjxUbnZXlBWXrOGCy-Rc130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1054799.RA6BqmSLYDDuezkp0WRFMXx1FKjxUbnZXlBWXrOGCy-Rc130_provenance.
• NP1054804.RAy6BK8_5TeRcnxO0AR4Ge4ybUoN1TbgflhjPANRx630A130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1054804.RAy6BK8_5TeRcnxO0AR4Ge4ybUoN1TbgflhjPANRx630A130_provenance.