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http://purl.uniprot.org/diseases/66http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/66http://www.w3.org/2000/01/rdf-schema#comment"A form of Aicardi-Goutieres syndrome, a genetically heterogeneous disease characterized by cerebral atrophy, leukoencephalopathy, intracranial calcifications, chronic cerebrospinal fluid (CSF) lymphocytosis, increased CSF alpha-interferon, and negative serologic investigations for common prenatal infection. Clinical features as thrombocytopenia, hepatosplenomegaly and elevated hepatic transaminases along with intermittent fever may erroneously suggest an infective process. Severe neurological dysfunctions manifest in infancy as progressive microcephaly, spasticity, dystonic posturing and profound psychomotor retardation. Death often occurs in early childhood."xsd:string
http://purl.uniprot.org/diseases/66http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/948
http://purl.uniprot.org/diseases/66http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/225750
http://purl.uniprot.org/diseases/66http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D009421
http://purl.uniprot.org/diseases/66http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D020274
http://purl.uniprot.org/diseases/66http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C0796126
http://purl.uniprot.org/diseases/66http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C3150315
http://purl.uniprot.org/diseases/66http://www.w3.org/2004/02/skos/core#prefLabel"Aicardi-Goutieres syndrome 1"xsd:string
http://purl.uniprot.org/diseases/66http://purl.uniprot.org/core/mnemonic"AGS1"xsd:string
http://purl.uniprot.org/diseases/66http://www.w3.org/2004/02/skos/core#altLabel"Cree encephalitis"xsd:string
http://purl.uniprot.org/diseases/66http://www.w3.org/2004/02/skos/core#altLabel"Pseudotoxoplasmosis syndrome"xsd:string
http://purl.uniprot.org/diseases/66http://www.w3.org/2004/02/skos/core#altLabel"Autosomal dominant Aicardi-Goutieres syndrome"xsd:string
http://purl.uniprot.org/diseases/66http://www.w3.org/2004/02/skos/core#altLabel"Pseudo-TORCH syndrome"xsd:string
http://purl.uniprot.org/diseases/66http://www.w3.org/2004/02/skos/core#altLabel"Encephalopathy familial infantile with intracranial calcification and chronic cerebrospinal fluid lymphocytosis"xsd:string
http://purl.uniprot.org/uniprot/Q9NSU2#SIP5F7A569253B74F2Fhttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/66
http://purl.uniprot.org/annotation/VAR_028319http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/66
http://purl.uniprot.org/annotation/VAR_028320http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/66
http://purl.uniprot.org/annotation/VAR_028321http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/66
http://purl.uniprot.org/annotation/VAR_032940http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/66
http://purl.uniprot.org/annotation/VAR_037948http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/66
http://purl.uniprot.org/annotation/VAR_070899http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/66
http://purl.uniprot.org/annotation/VAR_070900http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/66
http://purl.uniprot.org/annotation/VAR_070901http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/66
http://purl.uniprot.org/annotation/VAR_070902http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/66