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http://purl.uniprot.org/diseases/1031http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/1031http://www.w3.org/2000/01/rdf-schema#comment"An autosomal recessive neurocutaneous disorder characterized by a combination of severe intellectual disability, spastic di- or tetraplegia and congenital ichthyosis. Ichthyosis is usually evident at birth with varying degrees of erythema and scaling, neurologic symptoms appear in the first or second year of life. Most patients have an IQ of less than 60. Additional clinical features include glistening white spots on the retina, seizures, short stature and speech defects."xsd:string
http://purl.uniprot.org/diseases/1031http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/977
http://purl.uniprot.org/diseases/1031http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/991
http://purl.uniprot.org/diseases/1031http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/270200
http://purl.uniprot.org/diseases/1031http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D016111
http://purl.uniprot.org/diseases/1031http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C0037231
http://purl.uniprot.org/diseases/1031http://www.w3.org/2004/02/skos/core#prefLabel"Sjoegren-Larsson syndrome"xsd:string
http://purl.uniprot.org/diseases/1031http://purl.uniprot.org/core/mnemonic"SLS"xsd:string
http://purl.uniprot.org/uniprot/P51648#SIP2993D4612B3C7994http://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_002249http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_002250http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_002251http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_002252http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_002253http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_002254http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_002255http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_002256http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_017510http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_017511http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_017512http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_017513http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_017514http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_017515http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031
http://purl.uniprot.org/annotation/VAR_017516http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1031