@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:-PQTWS21G-M .

vh8: a skos:ConceptScheme .
vh8:-PQTWS21G-M
  skos:related vh8:-Z0NFZQS5-V ;
  skos:definition "Carnosinemia, is a rare autosomal recessive metabolic disorder caused by a deficiency of carnosinase', a dipeptidase (a type of enzyme that splits dipeptides into their two amino acid constituents).Carnosine is a dipeptide composed of beta-alanine and histidine, and is found in skeletal muscle and cells of the nervous system. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-W790N3DT-N ;
  skos:prefLabel "carnosinémie"@fr, "carnosinemia"@en ;
  skos:exactMatch <https://www.wikidata.org/wiki/Q4353825>, <https://en.wikipedia.org/wiki/Carnosinemia> .

vh8:-Z0NFZQS5-V
  skos:prefLabel "carnosine"@en, "carnosine"@fr ;
  a skos:Concept ;
  skos:related vh8:-PQTWS21G-M .