@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:-RCHS7MGL-7 .

vh8: a skos:ConceptScheme .
vh8:-C8B6KLHH-M
  skos:prefLabel "ENT disease"@en, "pathologie ORL"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-RCHS7MGL-7 .

vh8:-NNPJ6J5R-Q
  skos:prefLabel "pathologie de l'appareil génital mâle"@fr, "male genital diseases"@en ;
  a skos:Concept ;
  skos:narrower vh8:-RCHS7MGL-7 .

vh8:-RCHS7MGL-7
  skos:exactMatch <https://en.wikipedia.org/wiki/Opitz_G/BBB_syndrome> ;
  skos:broader vh8:-QG1RVCT9-L, vh8:-NNPJ6J5R-Q, vh8:-C0CS7VBM-F, vh8:-C8B6KLHH-M ;
  a skos:Concept ;
  skos:definition "Opitz G/BBB syndrome, also known as Opitz syndrome, G syndrome or BBB syndrome, is a rare genetic disorder that will affect physical structures along the midline of the body. (Wikipedia)"@en ;
  skos:inScheme vh8: ;
  skos:prefLabel "syndrome d'Opitz G/BBB"@fr, "Opitz G/BBB syndrome"@en .

vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-RCHS7MGL-7 .