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

vh8: a skos:ConceptScheme .
vh8:-K51SM8LZ-W
  skos:altLabel "partial 11q monosomy syndrome"@en ;
  skos:exactMatch <https://fr.wikipedia.org/wiki/Syndrome_de_Jacobsen>, <https://en.wikipedia.org/wiki/Jacobsen_syndrome> ;
  skos:prefLabel "Jacobsen syndrome"@en, "syndrome de Jacobsen"@fr ;
  skos:broader vh8:-TSXZX7B1-R, vh8:-F0Q8HP18-R ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:definition "Jacobsen syndrome is a rare chromosomal disorder resulting from deletion of genes from chromosome 11 that includes band 11q24.1. It is a congenital disorder. (Wikipedia)"@en .

vh8:-F0Q8HP18-R
  skos:prefLabel "malformation"@fr, "malformation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-K51SM8LZ-W .

vh8:-TSXZX7B1-R
  skos:prefLabel "chromosome C11 anormal"@fr, "abnormal chromosome C11"@en ;
  a skos:Concept ;
  skos:narrower vh8:-K51SM8LZ-W .