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

vh8:-BBV43VSG-5
  skos:prefLabel "dysplasie"@fr, "dysplasia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-VXSP9WQJ-7 .

vh8:-F0Q8HP18-R
  skos:prefLabel "malformation"@fr, "malformation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-VXSP9WQJ-7 .

vh8: a skos:ConceptScheme .
vh8:-VXSP9WQJ-7
  skos:inScheme vh8: ;
  skos:broader vh8:-BBV43VSG-5, vh8:-LFCRK960-N, vh8:-F0Q8HP18-R, vh8:-N32K7HZ8-D ;
  a skos:Concept ;
  skos:prefLabel "retinal dysplasia"@en, "dysplasie rétinienne"@fr ;
  skos:narrower vh8:-GFD1FH34-L ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Retinal_dysplasia> ;
  skos:definition "Retinal dysplasia is an eye disease affecting the retina of animals and, less commonly, humans. It is usually a nonprogressive disease and can be caused by viral infections, drugs, vitamin A deficiency, or genetic defects. (Wikipedia)"@en .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-VXSP9WQJ-7 .

vh8:-GFD1FH34-L
  skos:prefLabel "Walker-Warburg syndrome"@en, "syndrome de Walker et Warburg"@fr ;
  a skos:Concept ;
  skos:broader vh8:-VXSP9WQJ-7 .

vh8:-LFCRK960-N
  skos:prefLabel "retinopathy"@en, "rétinopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-VXSP9WQJ-7 .