@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:-NPK6R515-Z .

vh8: a skos:ConceptScheme .
vh8:-NPK6R515-Z
  skos:definition "Iminoglycinuria, is an autosomal recessive disorder of renal tubular transport affecting reabsorption of the amino acid glycine, and the imino acids proline and hydroxyproline. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-W790N3DT-N, vh8:-QT9H3FKW-K ;
  skos:prefLabel "iminoglycinurie"@fr, "iminoglycinuria"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Iminoglycinuria> .

vh8:-QT9H3FKW-K
  skos:prefLabel "tubulopathy"@en, "tubulopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-NPK6R515-Z .