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

vh8:-JFDJHJTQ-4
  skos:prefLabel "maladie congénitale"@fr, "congenital disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-T0PXSL0G-0 .

vh8:-T0PXSL0G-0
  a skos:Concept ;
  skos:prefLabel "cécité héréditaire de Norrie"@fr, "Norrie disease"@en ;
  skos:broader vh8:-LFCRK960-N, vh8:-HFVJ6MCG-6, vh8:-JFDJHJTQ-4, vh8:-G17S2R3L-V, vh8:-N32K7HZ8-D ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Norrie_disease>, <https://www.wikidata.org/wiki/Q1415842> ;
  skos:altLabel "maladie de Norrie"@fr ;
  skos:definition "Norrie disease is a genetic disorder that primarily affects the eye and almost always leads to blindness. (Wikipedia)"@en ;
  skos:inScheme vh8: .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-T0PXSL0G-0 .

vh8:-G17S2R3L-V
  skos:prefLabel "cécité"@fr, "blindness"@en ;
  a skos:Concept ;
  skos:narrower vh8:-T0PXSL0G-0 .

vh8:-HFVJ6MCG-6
  skos:prefLabel "nervous system diseases"@en, "pathologie du système nerveux"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-T0PXSL0G-0 .

vh8:-LFCRK960-N
  skos:prefLabel "retinopathy"@en, "rétinopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-T0PXSL0G-0 .