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

vh8:-PLFNN4S2-4
  skos:prefLabel "metabolic diseases"@en, "maladie métabolique"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-FKQ89NDG-V .

vh8:-G37XWGTK-R
  skos:prefLabel "enzymopathy"@en, "enzymopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-FKQ89NDG-V .

vh8:-C0CS7VBM-F
  skos:prefLabel "pathologie de l'oeil"@fr, "eye disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-FKQ89NDG-V .

vh8:-FKQ89NDG-V
  skos:broadMatch <https://en.wikipedia.org/wiki/Lecithin_cholesterol_acyltransferase_deficiency> ;
  skos:definition "Lecithin cholesterol acyltransferase deficiency is a disorder of lipoprotein metabolism. The disease has two forms: Familial LCAT deficiency, in which there is complete LCAT deficiency, and Fish-eye disease, in which there is a partial deficiency.Lecithin cholesterol acyltransferase catalyzes the formation of cholesterol esters in lipoproteins. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-G37XWGTK-R, vh8:-C0CS7VBM-F, vh8:-PLFNN4S2-4 ;
  skos:prefLabel "maladie de l'oeil de poisson"@fr, "fish-eye disease"@en .

vh8: a skos:ConceptScheme .