Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_provenance.
- NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_assertion wasGeneratedBy ECO_0000203 NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_provenance.
- NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_assertion wasDerivedFrom befree-20150227 NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_provenance.
- NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_assertion SIO_000772 20858596 NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_provenance.
- NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_assertion evidence source_evidence_literature NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_provenance.
- NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_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." NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_provenance.