Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP417104.RAdm4KNLBmQXnRZ8hV9D5a3UxLkfORfGmrOD655_w7XCg130_provenance.