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

<http://www.irandoc.acir/onto/irandoc/66091009>
  skos:prefLabel "بیماری مادرزادی"@fa, "Congenital disease"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  skos:narrower <http://www.irandoc.acir/onto/irandoc/763720007> .

<http://www.irandoc.acir/onto/irandoc/255399007>
  skos:prefLabel "مادرزادی"@fa, "Congenital"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept .

<http://rdf-vocabulary.ddialliance.org/xkos#Is_a> rdfs:label "هست یک"@fa, "Is a"@en .
<http://rdf-vocabulary.ddialliance.org/xkos#Occurrence> rdfs:label "وقوع"@fa, "Occurrence"@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/763720007> .

<http://www.irandoc.acir/onto/irandoc/763720007>
  skos:prefLabel "Hypermethioninemia due to deficiency of glycine N-methyltransferase"@en, "هیپر متیونینمی ناشی از کمبود گلیسین N متیل ترانسفراز"@fa ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/85995004>, <http://www.irandoc.acir/onto/irandoc/66091009>, "43123004" ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/85995004>, <http://www.irandoc.acir/onto/irandoc/66091009> ;
  ns0:Occurrence <http://www.irandoc.acir/onto/irandoc/255399007> ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept .