Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_assertion> ?p ?o ?g. }
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- NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_assertion type Assertion NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_head.
- 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.
- NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_assertion evidence source_evidence_literature NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_provenance.
- NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_assertion SIO_000772 25645926 NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_provenance.
- NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_assertion wasDerivedFrom befree-2016 NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_provenance.
- NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_assertion wasGeneratedBy ECO_0000203 NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_provenance.