Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_assertion type Assertion NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_head.
- NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_assertion wasGeneratedBy ECO_0000203 NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_provenance.
- NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_assertion wasDerivedFrom befree-20150227 NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_provenance.
- NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_assertion SIO_000772 20858596 NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_provenance.
- NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_assertion evidence source_evidence_literature NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_provenance.
- NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_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." NP887767.RAdoR3Xe-n22Z6pRK9UMUqzy6aWaL-UKMbeJHhKq65kM0130_provenance.