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

vh8:-TX6ZBC03-T
  skos:prefLabel "dysmorphie faciale"@fr, "dysmorphic facies"@en ;
  a skos:Concept ;
  skos:narrower vh8:-G4S53RZG-D .

vh8: a skos:ConceptScheme .
vh8:-FNLZG5GS-F
  skos:prefLabel "cognitive disorder"@en, "trouble cognitif"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-G4S53RZG-D .

vh8:-KH3C90B4-7
  skos:prefLabel "cardiopathie congénitale"@fr, "congenital heart disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-G4S53RZG-D .

vh8:-TSXZX7B1-R
  skos:prefLabel "chromosome C11 anormal"@fr, "abnormal chromosome C11"@en ;
  a skos:Concept ;
  skos:narrower vh8:-G4S53RZG-D .

vh8:-G4S53RZG-D
  skos:prefLabel "syndrome de Williams"@fr, "Williams syndrome"@en ;
  skos:exactMatch <https://www.wikidata.org/wiki/Q558077>, <https://fr.wikipedia.org/wiki/Syndrome_de_Williams>, <https://en.wikipedia.org/wiki/Williams_syndrome> ;
  skos:definition "Le syndrome de Williams (SW), ou de Williams et Beuren, est l’association d’un retard mental, d’une cardiopathie congénitale, d’un faciès et d’un comportement caractéristiques de l’individu affecté. (Wikipédia)"@fr, "Williams syndrome (WS) is a genetic disorder that affects many parts of the body. Facial features frequently include a broad forehead, short nose and full cheeks, an appearance that has been described as \"elfin\". (Wikipedia)"@en ;
  a skos:Concept ;
  skos:broader vh8:-KH3C90B4-7, vh8:-TX6ZBC03-T, vh8:-FNLZG5GS-F, vh8:-TSXZX7B1-R, vh8:-JW4BV3J7-L ;
  skos:altLabel "syndrome de Williams-Beuren"@fr, "Williams-Beuren syndrome"@en ;
  skos:inScheme vh8: .

vh8:-JW4BV3J7-L
  skos:prefLabel "arriération mentale"@fr, "mental retardation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-G4S53RZG-D .