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http://purl.uniprot.org/diseases/5347http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/5347http://www.w3.org/2000/01/rdf-schema#comment"An autosomal recessive disorder with onset in utero or early infancy and characterized by severe global developmental delay, seizures, hypotonia, weakness, ataxia, and dysmorphic facial features."xsd:string
http://purl.uniprot.org/diseases/5347http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/887
http://purl.uniprot.org/diseases/5347http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/618143
http://purl.uniprot.org/diseases/5347http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D008607
http://purl.uniprot.org/diseases/5347http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/CN257729
http://purl.uniprot.org/diseases/5347http://www.w3.org/2004/02/skos/core#prefLabel"Glycosylphosphatidylinositol biosynthesis defect 18"xsd:string
http://purl.uniprot.org/diseases/5347http://purl.uniprot.org/core/mnemonic"GPIBD18"xsd:string
http://purl.uniprot.org/uniprot/Q96S52#SIP09F36EDBC74DA9BBhttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/5347
http://purl.uniprot.org/annotation/VAR_081579http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/5347
http://purl.uniprot.org/annotation/VAR_081580http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/5347
http://purl.uniprot.org/annotation/VAR_081581http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/5347
http://purl.uniprot.org/annotation/VAR_081582http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/5347
http://purl.uniprot.org/uniprot/#_5CC75F44DBAD71C2_up.disease_1DA9244A1FF5F7E4http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/5347