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

vh8:-W790N3DT-N
  skos:prefLabel "aminoacid disorder"@en, "aminoacidopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-R3PTDNQX-0 .

vh8: a skos:ConceptScheme .
vh8:-R3PTDNQX-0
  skos:definition "3-Hydroxy-3-methylglutaryl-CoA lyase deficiency is an uncommon inherited disorder in which the body cannot properly process the amino acid leucine. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-W790N3DT-N ;
  skos:prefLabel "déficit en 3-hydroxy-3-méthylglutaryl-CoA lyase"@fr, "3-hydroxy-3 methylglutaryl-CoA lyase deficiency"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/3-Hydroxy-3-methylglutaryl-CoA_lyase_deficiency> .