Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP610849.RACl14xbQiH5rpv8e89WVZPRzHLifzjqw6dxsnwRFFXz4130_provenance.