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http://purl.uniprot.org/diseases/1161http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/1161http://www.w3.org/2000/01/rdf-schema#comment"An autosomal recessive pigmentary skin disorder characterized by solar hypersensitivity of the skin, high predisposition for developing cancers on areas exposed to sunlight and, in some cases, neurological abnormalities. The skin develops marked freckling and other pigmentation abnormalities. Some XP-G patients present features of Cockayne syndrome, cachectic dwarfism, pigmentary retinopathy, ataxia, decreased nerve conduction velocities. The phenotype combining xeroderma pigmentosum and Cockayne syndrome traits is referred to as XP-CS complex."xsd:string
http://purl.uniprot.org/diseases/1161http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/857
http://purl.uniprot.org/diseases/1161http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/172
http://purl.uniprot.org/diseases/1161http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/278780
http://purl.uniprot.org/diseases/1161http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D014983
http://purl.uniprot.org/diseases/1161http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C0268141
http://purl.uniprot.org/diseases/1161http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C1851443
http://purl.uniprot.org/diseases/1161http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C1968561
http://purl.uniprot.org/diseases/1161http://www.w3.org/2004/02/skos/core#prefLabel"Xeroderma pigmentosum complementation group G"xsd:string
http://purl.uniprot.org/diseases/1161http://purl.uniprot.org/core/mnemonic"XP-G"xsd:string
http://purl.uniprot.org/diseases/1161http://www.w3.org/2004/02/skos/core#altLabel"XP group G"xsd:string
http://purl.uniprot.org/diseases/1161http://www.w3.org/2004/02/skos/core#altLabel"XP-G/CS"xsd:string
http://purl.uniprot.org/diseases/1161http://www.w3.org/2004/02/skos/core#altLabel"XP7"xsd:string
http://purl.uniprot.org/diseases/1161http://www.w3.org/2004/02/skos/core#altLabel"Xeroderma pigmentosum VII"xsd:string
http://purl.uniprot.org/uniprot/P28715#SIP6D04B811B4D96FC2http://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/1161
http://purl.uniprot.org/annotation/VAR_007733http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1161
http://purl.uniprot.org/annotation/VAR_015280http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1161
http://purl.uniprot.org/annotation/VAR_017096http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1161
http://purl.uniprot.org/annotation/VAR_017097http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1161
http://purl.uniprot.org/annotation/VAR_075773http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1161
http://purl.uniprot.org/annotation/VAR_075774http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1161
http://purl.uniprot.org/uniprot/#_FE761C15D1F590E0_up.disease_6437D6428AEDBE7Fhttp://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/1161