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

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-BB6SW476-B .

vh8:-BB6SW476-B
  skos:broader vh8:-MF2505S3-R, vh8:-N32K7HZ8-D, vh8:-TD24TNVJ-V ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Infantile_neuroaxonal_dystrophy> ;
  a skos:Concept ;
  skos:altLabel "maladie de Seitelberger"@fr ;
  skos:narrower vh8:-LCL2PB9W-6 ;
  skos:definition "Infantile neuroaxonal dystrophy is a rare pervasive developmental disorder that primarily affects the nervous system. (Wikipedia)"@en ;
  skos:inScheme vh8: ;
  skos:prefLabel "dystrophie neuroaxonale"@fr, "neuroaxonal dystrophy"@en .

vh8:-LCL2PB9W-6
  skos:prefLabel "maladie de Hallervorden-Spatz"@fr, "Hallervorden-Spatz disease"@en ;
  a skos:Concept ;
  skos:broader vh8:-BB6SW476-B .

vh8:-TD24TNVJ-V
  skos:prefLabel "dystrophie"@fr, "dystrophy"@en ;
  a skos:Concept ;
  skos:narrower vh8:-BB6SW476-B .

vh8:-MF2505S3-R
  skos:prefLabel "pathologie de l'encéphale"@fr, "cerebral disorder"@en ;
  a skos:Concept ;
  skos:narrower vh8:-BB6SW476-B .