Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_assertion type Assertion NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_head.
- NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_assertion description "[We used magnetic resonance imaging (MRI) to show that individuals with aniridia and deficits in executive and social cognition, due to heterozygous mutation of the neurodevelopmental control gene PAX6, have structural abnormalities of grey matter in anterior cingulate cortex, cerebellum and medial temporal lobe, as well as white matter deficits in corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_provenance.
- NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_assertion evidence source_evidence_literature NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_provenance.
- NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_assertion SIO_000772 15066147 NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_provenance.
- NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_assertion wasDerivedFrom befree-20140225 NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_provenance.
- NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_assertion wasGeneratedBy ECO_0000203 NP615528.RATL5TeW8gxCqFxslE7KY5jVdyTjW9ZANOOhTklMHo2dE130_provenance.