Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_assertion> ?p ?o ?g. }
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- NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_assertion type Assertion NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_head.
- 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.
- NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_assertion evidence source_evidence_literature NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_provenance.
- NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_assertion SIO_000772 16302874 NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_provenance.
- NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_assertion wasDerivedFrom befree-20140225 NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_provenance.
- NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_assertion wasGeneratedBy ECO_0000203 NP163293.RANYYX3gh8WdKWjpuAvaY35_NPdRrQN-9DOkgtP6lFkuw130_provenance.