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

vh8:-C0CS7VBM-F
  skos:prefLabel "pathologie de l'oeil"@fr, "eye disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-SKWSL2D0-1 .

vh8: a skos:ConceptScheme .
vh8:-F0Q8HP18-R
  skos:prefLabel "malformation"@fr, "malformation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-SKWSL2D0-1 .

vh8:-SKWSL2D0-1
  skos:definition "Axenfeld syndrome is a rare autosomal dominant disorder, which affects the development of the teeth, eyes, and abdominal region. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-C0CS7VBM-F, vh8:-F0Q8HP18-R ;
  skos:prefLabel "syndrome d'Axenfeld"@fr, "Axenfeld syndrome"@en ;
  skos:altLabel "embryotoxon postérieur"@fr ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Axenfeld_syndrome> .