Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_assertion> ?p ?o ?g. }
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- NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_assertion type Assertion NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_head.
- NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_assertion description "[In conclusion, mutations in GABRA1, GABRB2 and GABRG2 do not seem to be a major genetic cause of epilepsy with typical and atypical absences in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_provenance.
- NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_assertion evidence source_evidence_literature NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_provenance.
- NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_assertion SIO_000772 15955415 NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_provenance.
- NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_assertion wasDerivedFrom befree-20140225 NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_provenance.
- NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_assertion wasGeneratedBy ECO_0000203 NP322519.RAKs8IbeMlsUvIZUupyUEXolwR4Omk-Xw53x4YzSpqNqk130_provenance.