Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_assertion> ?p ?o ?g. }
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- NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_assertion type Assertion NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_head.
- NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_provenance.
- NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_assertion evidence source_evidence_literature NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_provenance.
- NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_assertion SIO_000772 10826984 NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_provenance.
- NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_assertion wasDerivedFrom befree-20150227 NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_provenance.
- NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_assertion wasGeneratedBy ECO_0000203 NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_provenance.