Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_assertion> ?p ?o ?g. }
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- NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_assertion type Assertion NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_head.
- NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_assertion wasGeneratedBy ECO_0000203 NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_provenance.
- NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_assertion wasDerivedFrom befree-20140225 NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_provenance.
- NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_assertion SIO_000772 20858596 NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_provenance.
- NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_assertion evidence source_evidence_literature NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_provenance.
- NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_assertion description "[Mutations in transcription factor FOXP2 cause difficulties mastering fluent speech (developmental verbal dyspraxia, DVD), whereas mutations of sushi-repeat protein SRPX2 lead to epilepsy of the rolandic (sylvian) speech areas, with DVD or with bilateral perisylvian polymicrogyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_provenance.