Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_assertion> ?p ?o ?g. }
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- NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_assertion type Assertion NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_head.
- 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.
- NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_assertion evidence source_evidence_literature NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_provenance.
- NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_assertion SIO_000772 16302874 NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_provenance.
- NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_assertion wasDerivedFrom befree-20150227 NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_provenance.
- NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_assertion wasGeneratedBy ECO_0000203 NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_provenance.