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

vh8:-K4G2JJ0L-5
  skos:prefLabel "dystrophie musculaire"@fr, "muscular dystrophy"@en ;
  a skos:Concept ;
  skos:narrower vh8:-GFD1FH34-L .

vh8: a skos:ConceptScheme .
vh8:-VXSP9WQJ-7
  skos:prefLabel "dysplasie rétinienne"@fr, "retinal dysplasia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-GFD1FH34-L .

vh8:-JZ7N6WGB-5
  skos:prefLabel "hypotonie"@fr, "hypotonia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-GFD1FH34-L .

vh8:-TKQ949DD-T
  skos:prefLabel "hydrocéphalie"@fr, "hydrocephaly"@en ;
  a skos:Concept ;
  skos:narrower vh8:-GFD1FH34-L .

vh8:-SG5CCPDX-0
  skos:prefLabel "lissencephaly"@en, "lissencéphalie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-GFD1FH34-L .

vh8:-TT4GBZDF-H
  skos:prefLabel "retard psychomoteur"@fr, "psychomotor retardation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-GFD1FH34-L .

vh8:-GFD1FH34-L
  skos:broader vh8:-VXSP9WQJ-7, vh8:-TKQ949DD-T, vh8:-JZ7N6WGB-5, vh8:-SG5CCPDX-0, vh8:-K4G2JJ0L-5, vh8:-TT4GBZDF-H ;
  skos:inScheme vh8: ;
  skos:prefLabel "syndrome de Walker et Warburg"@fr, "Walker-Warburg syndrome"@en ;
  skos:definition "Walker–Warburg syndrome (WWS), also called Warburg syndrome, Chemke syndrome, HARD syndrome (Hydrocephalus, Agyria and Retinal Dysplasia), Pagon syndrome, cerebroocular dysgenesis (COD) or cerebroocular dysplasia-muscular dystrophy syndrome (COD-MD), is a rare form of autosomal recessive congenital muscular dystrophy. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Walker%E2%80%93Warburg_syndrome> .