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

vh8:-D54M42MR-9
  skos:definition "Multi/minicore myopathy is a congenital myopathy usually caused by mutations in either the SEPN1 and RYR1 genes. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-KXDKK4T8-H, vh8:-JFDJHJTQ-4 ;
  skos:prefLabel "myopathie à multicore"@fr, "multicore myopathy"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Multi/minicore_myopathy> .

vh8: a skos:ConceptScheme .
vh8:-KXDKK4T8-H
  skos:prefLabel "myopathie"@fr, "myopathy"@en ;
  a skos:Concept ;
  skos:narrower vh8:-D54M42MR-9 .

vh8:-JFDJHJTQ-4
  skos:prefLabel "maladie congénitale"@fr, "congenital disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-D54M42MR-9 .