Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_assertion type Assertion NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_head.
- NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_assertion description "[Deletion of the LIMK1 gene is associated with Williams syndrome, a unique neurodevelopmental disorder characterized by severe defects in visuospatial cognition and long-term memory (LTM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_provenance.
- NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_assertion evidence source_evidence_literature NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_provenance.
- NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_assertion SIO_000772 25645926 NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_provenance.
- NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_assertion wasDerivedFrom befree-2016 NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_provenance.
- NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_assertion wasGeneratedBy ECO_0000203 NP1260482.RABPilQEbuAVFYNqP20T7bAGY5G8xfXWmluxNuvMXgK0M130_provenance.