Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_assertion type Assertion NP887794.RAFMv5byG0ASZvHGYUEy3ZQsdznx1q4QUejYbh3hU9KNg130_head.
- 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.