Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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." provenance.
- 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." provenance.
- 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.
- NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_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." NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_provenance.