@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix ns0: <http://rdf-vocabulary.ddialliance.org/xkos#> .

<http://rdf-vocabulary.ddialliance.org/xkos#Is_a> rdfs:label "هست یک"@fa, "Is a"@en .
<http://rdf-vocabulary.ddialliance.org/xkos#Due_to> rdfs:label "به دلیل"@fa, "Due to"@en .
<http://www.irandoc.acir/onto/irandoc/85995004>
  skos:prefLabel "اختلال ارثی مغلوب، NOS"@fa, "Recessive hereditary disorder, NOS"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  skos:narrower <http://www.irandoc.acir/onto/irandoc/717181004> .

<http://www.irandoc.acir/onto/irandoc/124177001>
  skos:prefLabel "کمبود پیرولین 5 کربوکسیلات ردوکتاز"@fa, "Deficiency of pyrroline-5-carboxylate reductase"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept .

<http://www.irandoc.acir/onto/irandoc/717181004>
  ns0:Due_to <http://www.irandoc.acir/onto/irandoc/124177001> ;
  ns0:Is_a "59655002", <http://www.irandoc.acir/onto/irandoc/85995004> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/85995004> ;
  skos:prefLabel "هیپرپرولینمی نوع 2 (اختلال)"@fa, "Hyperprolinemia type 2 (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept .

