@prefix n9j: <http://data.loterre.fr/ark:/67375/N9J> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix isothes: <http://purl.org/iso25964/skos-thes#> .

n9j:-D1L019LH-F
  skos:prefLabel "chromosome inversion"@en ;
  a skos:Concept ;
  skos:broader n9j:-VMT0H494-3 .

n9j:-TS1QGQ0P-S
  skos:prefLabel "polyploidy"@en ;
  a skos:Concept ;
  skos:broader n9j:-VMT0H494-3 .

n9j:-S1669T7K-X
  skos:prefLabel "trisomy"@en ;
  a skos:Concept ;
  skos:broader n9j:-VMT0H494-3 .

n9j:-Q4MN1NKL-H
  skos:prefLabel "aneuploidy"@en ;
  a skos:Concept ;
  skos:broader n9j:-VMT0H494-3 .

n9j:-NRRK4WF1-4
  skos:prefLabel "Prader-Willi syndrome"@en ;
  a skos:Concept ;
  skos:broader n9j:-VMT0H494-3 .

n9j: a skos:ConceptScheme .
n9j:-X86BZKHG-V
  skos:prefLabel "autosome abnormalities"@en ;
  a skos:Concept ;
  skos:broader n9j:-VMT0H494-3 .

n9j:-VMT0H494-3
  skos:inScheme n9j: ;
  skos:narrower n9j:-NRRK4WF1-4, n9j:-S1669T7K-X, n9j:-G9D845J5-2, n9j:-D1L019LH-F, n9j:-Q4MN1NKL-H, n9j:-TS1QGQ0P-S, n9j:-FJ6GFG5X-K, n9j:-LGDLB4SZ-X, n9j:-X86BZKHG-V ;
  a skos:Concept ;
  skos:broader n9j:-PNHQWTC5-V ;
  skos:prefLabel "chromosome abnormalities"@en ;
  owl:sameAs <https://concepts.sagepub.com/social-science/concept/chromosome_abnormalities> .

n9j:-concepts
  a isothes:ConceptGroup ;
  skos:prefLabel "concepts"@en ;
  skos:member n9j:-VMT0H494-3 .

n9j:-PNHQWTC5-V
  skos:prefLabel "genetic disorders"@en ;
  a skos:Concept ;
  skos:narrower n9j:-VMT0H494-3 .

n9j:-FJ6GFG5X-K
  skos:prefLabel "chromosome nondisjunction"@en ;
  a skos:Concept ;
  skos:broader n9j:-VMT0H494-3 .

n9j:-LGDLB4SZ-X
  skos:prefLabel "Fragile X syndrome"@en ;
  a skos:Concept ;
  skos:broader n9j:-VMT0H494-3 .

n9j:-G9D845J5-2
  skos:prefLabel "chromosome translocation"@en ;
  a skos:Concept ;
  skos:broader n9j:-VMT0H494-3 .