@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:-HGVJ2CLT-K
  skos:prefLabel "cri-du-chat syndrome"@en ;
  a skos:Concept ;
  skos:broader n9j:-NN485M62-1 .

n9j:-SX7MH6J4-D
  skos:prefLabel "Down syndrome"@en ;
  a skos:Concept ;
  skos:broader n9j:-NN485M62-1 .

n9j:-NN485M62-1
  skos:narrower n9j:-BGKVS0MM-X, n9j:-HGVJ2CLT-K, n9j:-XSFH6TT4-Q, n9j:-TZMRNZF9-9, n9j:-SX7MH6J4-D, n9j:-NRRK4WF1-4 ;
  a skos:Concept ;
  skos:inScheme n9j: ;
  skos:broader n9j:-LHW2SN10-S ;
  skos:definition "We are often taught that what makes us male or female is our genetics, particularly our chromosomes. Typically, a person has 23 pairs of chromosomes; one half comes from the egg, and the other half from the sperm. [Source: Encyclopedia of Gender and Society; Chromosome Disorders]"@en ;
  owl:sameAs <https://concepts.sagepub.com/social-science/concept/chromosome_disorders> ;
  skos:prefLabel "chromosome disorders"@en .

n9j:-XSFH6TT4-Q
  skos:prefLabel "Wagr syndrome"@en ;
  a skos:Concept ;
  skos:broader n9j:-NN485M62-1 .

n9j:-NRRK4WF1-4
  skos:prefLabel "Prader-Willi syndrome"@en ;
  a skos:Concept ;
  skos:broader n9j:-NN485M62-1 .

n9j: a skos:ConceptScheme .
n9j:-LHW2SN10-S
  skos:prefLabel "gender and health"@en ;
  a skos:Concept ;
  skos:narrower n9j:-NN485M62-1 .

n9j:-TZMRNZF9-9
  skos:prefLabel "Cornelia de Lange Syndrome"@en ;
  a skos:Concept ;
  skos:broader n9j:-NN485M62-1 .

n9j:-BGKVS0MM-X
  skos:prefLabel "Rubinstein-Taybi syndrome"@en ;
  a skos:Concept ;
  skos:broader n9j:-NN485M62-1 .

n9j:-concepts
  a isothes:ConceptGroup ;
  skos:prefLabel "concepts"@en ;
  skos:member n9j:-NN485M62-1 .