Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_assertion> ?p ?o ?g. }
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- NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_assertion type Assertion NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_head.
- 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.
- NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_assertion evidence source_evidence_literature NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_provenance.
- NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_assertion SIO_000772 16302874 NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_provenance.
- NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_assertion wasDerivedFrom befree-20140225 NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_provenance.
- NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_assertion wasGeneratedBy ECO_0000203 NP725472.RAtw1z8-CCNocUFSABH7XaJbU4i5GhwdwVdSxj9KfZYIk130_provenance.