Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_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.
- 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.
- befree-2016 importedOn "2016-02-19" NP1260481.RAyWPYHApqzk_FaM1PoQWSnswyxpP6jZ8a2K8_1szo9NI130_provenance.