@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:-X616F87X-3 .

vh8:-X616F87X-3
  skos:definition "Hyperlysinemia is an autosomal recessive metabolic disorder characterized by an abnormal increase of lysine in the blood, but appears to be benign. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-W790N3DT-N, vh8:-XZJTZ9TJ-J ;
  skos:prefLabel "hyperlysinémie"@fr, "hyperlysinemia"@en ;
  skos:exactMatch <https://www.wikidata.org/wiki/Q13637039>, <https://en.wikipedia.org/wiki/Hyperlysinemia> .

vh8: a skos:ConceptScheme .
vh8:-XZJTZ9TJ-J
  skos:prefLabel "biological abnormality"@en, "anomalie biologique"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-X616F87X-3 .