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http://purl.uniprot.org/diseases/5101http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/5101http://www.w3.org/2000/01/rdf-schema#comment"An autosomal dominant neurodegenerative disease with onset in childhood, characterized by progressive cortical atrophy, developmental delay, developmental regression, loss of motor skills and ambulation, absence of language, and intellectual disability."xsd:string
http://purl.uniprot.org/diseases/5101http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/523
http://purl.uniprot.org/diseases/5101http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/991
http://purl.uniprot.org/diseases/5101http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/617672
http://purl.uniprot.org/diseases/5101http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D019636
http://purl.uniprot.org/diseases/5101http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/CN469330
http://purl.uniprot.org/diseases/5101http://www.w3.org/2004/02/skos/core#prefLabel"Neurodegeneration, childhood-onset, with brain atrophy"xsd:string
http://purl.uniprot.org/diseases/5101http://purl.uniprot.org/core/mnemonic"CONDBA"xsd:string
http://purl.uniprot.org/uniprot/P17480#SIP5C69E4C48589660Bhttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/5101
http://purl.uniprot.org/annotation/VAR_080139http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/5101
http://purl.uniprot.org/uniprot/#_3C6A326A87A26717_up.disease_009E6F1331AA4439http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/5101