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

vh8:-R2PS9LZZ-S
  skos:definition "Systemic primary carnitine deficiency (SPCD), is an inborn error of fatty acid transport caused by a defect in the transporter responsible for moving carnitine across the plasma membrane. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-PLFNN4S2-4 ;
  skos:prefLabel "carnitine deficiency"@en, "déficit en carnitine"@fr ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Systemic_primary_carnitine_deficiency> .

vh8: a skos:ConceptScheme .
vh8:-PLFNN4S2-4
  skos:prefLabel "metabolic diseases"@en, "maladie métabolique"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-R2PS9LZZ-S .

