@prefix vh8: <http://data.loterre.fr/ark:/67375/VH8> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .

vh8:-SP5NMVCZ-1
  skos:broader vh8:-C0CS7VBM-F, vh8:-LWHFH8W7-W, vh8:-M7X3NL2G-F, vh8:-N32K7HZ8-D, vh8:-DWZ6Z6N8-Q, vh8:-NHM2Q2Q1-9 ;
  skos:definition "L'ataxie télangiectasie, aussi nommée syndrome de Louis-Bar (code CIM-10 : G11.3), est une maladie génétique autosomique récessive. (Wikipédia)"@fr, "Ataxia–telangiectasia (AT or A–T), also referred to as ataxia–telangiectasia syndrome or Louis–Bar syndrome, is a rare, neurodegenerative, autosomal recessive disease causing severe disability. (Wikipedia)"@en ;
  skos:exactMatch <https://www.wikidata.org/wiki/Q387082>, <https://en.wikipedia.org/wiki/Ataxia%E2%80%93telangiectasia>, <https://fr.wikipedia.org/wiki/Ataxie_t%C3%A9langiectasie> ;
  skos:altLabel "syndrome de Louis-Bar"@fr ;
  skos:prefLabel "ataxie télangiectasie"@fr, "ataxia telangiectasia"@en ;
  a skos:Concept ;
  skos:inScheme vh8: .

vh8:-C0CS7VBM-F
  skos:prefLabel "pathologie de l'oeil"@fr, "eye disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-SP5NMVCZ-1 .

vh8:-NHM2Q2Q1-9
  skos:prefLabel "cerebellar ataxia"@en, "ataxie cérébelleuse"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-SP5NMVCZ-1 .

vh8: a skos:ConceptScheme .
vh8:-M7X3NL2G-F
  skos:prefLabel "pathologie de la peau"@fr, "skin disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-SP5NMVCZ-1 .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-SP5NMVCZ-1 .

vh8:-LWHFH8W7-W
  skos:prefLabel "télangiectasie"@fr, "telangiectasia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-SP5NMVCZ-1 .

vh8:-DWZ6Z6N8-Q
  skos:prefLabel "immunopathologie"@fr, "immunopathology"@en ;
  a skos:Concept ;
  skos:narrower vh8:-SP5NMVCZ-1 .