Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_assertion> ?p ?o ?g. }
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- NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_assertion type Assertion NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_head.
- 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.
- NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_assertion evidence source_evidence_literature NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_provenance.
- NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_assertion SIO_000772 23429546 NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_provenance.
- NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_assertion wasDerivedFrom befree-20140225 NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_provenance.
- NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_assertion wasGeneratedBy ECO_0000203 NP322608.RAVT4XZCLJIOMjf9ANYN1MsvMedIHoaN3NqghBOpQsReE130_provenance.