| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Disease |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2000/01/rdf-schema#comment | "An early-onset progressive neurodegenerative disorder characterized by the presence of focal, bilateral lesions in one or more areas of the central nervous system including the brainstem, thalamus, basal ganglia, cerebellum and spinal cord. Clinical features depend on which areas of the central nervous system are involved and include subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, vision loss, eye movement abnormalities, seizures, and dysphagia."xsd:string |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/keywords/431 |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/mim/256000 |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://id.nlm.nih.gov/mesh/D007888 |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/medgen/C0023264 |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/medgen/C1838951 |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/medgen/C1850597 |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/medgen/C1850598 |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/medgen/C1850600 |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/medgen/C2931891 |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2004/02/skos/core#prefLabel | "Leigh syndrome"xsd:string |
| http://purl.uniprot.org/diseases/1886 | http://purl.uniprot.org/core/mnemonic | "LS"xsd:string |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2004/02/skos/core#altLabel | "SNE"xsd:string |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2004/02/skos/core#altLabel | "Leigh syndrome due to mitochondrial complex V deficiency"xsd:string |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2004/02/skos/core#altLabel | "Necrotizing encephalopathy infantile subacute of Leigh"xsd:string |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2004/02/skos/core#altLabel | "Leigh syndrome due to mitochondrial complex IV deficiency"xsd:string |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2004/02/skos/core#altLabel | "Leigh Disease"xsd:string |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2004/02/skos/core#altLabel | "Leigh syndrome due to mitochondrial complex III deficiency"xsd:string |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2004/02/skos/core#altLabel | "Leigh syndrome due to mitochondrial complex I deficiency"xsd:string |
| http://purl.uniprot.org/diseases/1886 | http://www.w3.org/2004/02/skos/core#altLabel | "Leigh syndrome due to mitochondrial complex II deficiency"xsd:string |
| http://purl.uniprot.org/uniprot/P00846#SIPE11C5136D14161F2 | http://purl.uniprot.org/core/disease | http://purl.uniprot.org/diseases/1886 |
| http://purl.uniprot.org/uniprot/P54098#SIP17E76004D7229243 | http://purl.uniprot.org/core/disease | http://purl.uniprot.org/diseases/1886 |
| http://purl.uniprot.org/uniprot/P03923#SIP012B4E8477CDBA26 | http://purl.uniprot.org/core/disease | http://purl.uniprot.org/diseases/1886 |
| http://purl.uniprot.org/uniprot/P03891#SIP4175DDCDB7CF0526 | http://purl.uniprot.org/core/disease | http://purl.uniprot.org/diseases/1886 |