Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_assertion> ?p ?o ?g. }
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- NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_assertion description "[Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718590.RAQUCXpnpnGVqjNbEZ5041msHI9mZb0MwPyPY_Drrp53U130_provenance.
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