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

vh8:-QK89WK24-9
  skos:prefLabel "dysplasie fibreuse"@fr, "fibrous dysplasia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-N0TV41R3-N .

vh8:-DP00LHWS-H
  skos:prefLabel "puberté précoce"@fr, "precocious puberty"@en ;
  a skos:Concept ;
  skos:narrower vh8:-N0TV41R3-N .

vh8: a skos:ConceptScheme .
vh8:-CZGBG75B-L
  skos:prefLabel "osteochondrodysplasia"@en, "ostéochondrodysplasie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-N0TV41R3-N .

vh8:-GQ6VT558-G
  skos:prefLabel "pseudohypoparathyroïdie"@fr, "pseudohypoparathyroidism"@en ;
  a skos:Concept ;
  skos:narrower vh8:-N0TV41R3-N .

vh8:-HSZJBJW6-W
  skos:prefLabel "pigmentation disorder"@en, "trouble de la pigmentation"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-N0TV41R3-N .

vh8:-N0TV41R3-N
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-GQ6VT558-G, vh8:-QK89WK24-9, vh8:-HSZJBJW6-W, vh8:-DP00LHWS-H, vh8:-CZGBG75B-L ;
  skos:prefLabel "syndrome d'Albright"@fr, "Albright disease"@en .