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

vh8:-G37XWGTK-R
  skos:prefLabel "enzymopathy"@en, "enzymopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-RVZ3P800-W .

vh8: a skos:ConceptScheme .
vh8:-Z7HB6W2K-N
  skos:prefLabel "hyperuricémie"@fr, "hyperuricemia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-RVZ3P800-W .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-RVZ3P800-W .

vh8:-RVZ3P800-W
  skos:inScheme vh8: ;
  skos:broader vh8:-JW4BV3J7-L, vh8:-TPQPXQG0-K, vh8:-W18ZM1GK-S, vh8:-Z7HB6W2K-N, vh8:-G37XWGTK-R, vh8:-N32K7HZ8-D ;
  a skos:Concept ;
  skos:definition "Lesch–Nyhan syndrome (LNS), is a rare inherited disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT). (Wikipedia)"@en ;
  skos:prefLabel "Lesch-Nyhan syndrome"@en, "syndrome de Lesh et Nyhan"@fr ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Lesch%E2%80%93Nyhan_syndrome>, <https://www.wikidata.org/wiki/Q727436> .

vh8:-W18ZM1GK-S
  skos:prefLabel "automutilation"@fr, "self-injury"@en ;
  a skos:Concept ;
  skos:narrower vh8:-RVZ3P800-W .

vh8:-TPQPXQG0-K
  skos:prefLabel "choréoathétose"@fr, "choreoathetosis"@en ;
  a skos:Concept ;
  skos:narrower vh8:-RVZ3P800-W .

vh8:-JW4BV3J7-L
  skos:prefLabel "arriération mentale"@fr, "mental retardation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-RVZ3P800-W .