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

<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://www.irandoc.acir/onto/irandoc/308490002>
  skos:prefLabel "فرآیند رشد پاتولوژیک"@fa, "Pathological developmental process"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept .

<http://www.irandoc.acir/onto/irandoc/49755003>
  skos:prefLabel "ناهنجاری مورفولوژیک"@fa, "Morphologic abnormality"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept .

<http://www.irandoc.acir/onto/irandoc/127954009>
  skos:prefLabel "skeletal muscle"@en, "عضله اسکلتی"@fa ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept .

<http://www.irandoc.acir/onto/irandoc/770786001>
  skos:prefLabel "میوپاتی با انکلوژن ارثی نوع 4 (اختلال)"@fa, "Hereditary inclusion body myopathy type 4 (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/240086009> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/240086009> .

<http://www.irandoc.acir/onto/irandoc/719815005>
  skos:prefLabel "میوپاتی مرتبط X با اتوفاژی بیش از حد (اختلال)"@fa, "X-linked myopathy with excessive autophagy (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/240086009> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/240086009> .

<http://www.irandoc.acir/onto/irandoc/715646003>
  skos:prefLabel "میوپاتی مرتبط با دسمین با انکلوزیون های بدن مالوری (اختلال)"@fa, "Desmin related myopathy with Mallory body-like inclusions (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/240086009> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/240086009> .

<http://www.irandoc.acir/onto/irandoc/702382000>
  skos:prefLabel "میوپاتی بدن انکلوژن ارثی"@fa, "Hereditary inclusion body myopathy"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/240086009> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/240086009> .

ns0:Is_a rdfs:label "هست یک"@fa, "Is a"@en .
<http://www.irandoc.acir/onto/irandoc/770627003>
  skos:prefLabel "میوپاتی میوفیبریلار مرتبط با دسمین (اختلال)"@fa, "Desmin-related myofibrillar myopathy (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/240086009> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/240086009> .

<http://www.irandoc.acir/onto/irandoc/240086009>
  ns0:Pathological_process <http://www.irandoc.acir/onto/irandoc/308490002> ;
  skos:narrower <http://www.irandoc.acir/onto/irandoc/770627003>, <http://www.irandoc.acir/onto/irandoc/715646003>, <http://www.irandoc.acir/onto/irandoc/703544004>, <http://www.irandoc.acir/onto/irandoc/724349009>, <http://www.irandoc.acir/onto/irandoc/719815005>, <http://www.irandoc.acir/onto/irandoc/770786001>, <http://www.irandoc.acir/onto/irandoc/702382000> ;
  skos:prefLabel "Myopathy with cytoplasmic inclusions"@en, "میوپاتی با ادخال سیتوپلاسمی"@fa ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/89886004> ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Associated_morphology <http://www.irandoc.acir/onto/irandoc/49755003> ;
  ns0:Occurrence <http://www.irandoc.acir/onto/irandoc/255399007> ;
  ns0:Finding_site <http://www.irandoc.acir/onto/irandoc/127954009> ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/89886004> .

ns0:Associated_morphology rdfs:label "مورفولوژی مرتبط"@fa, "Associated morphology"@en .
ns0:Occurrence rdfs:label "وقوع"@fa, "Occurrence"@en .
<http://www.irandoc.acir/onto/irandoc/724349009>
  skos:prefLabel "میوپاتی با انکلوژن ارثی، انقباض مفصل، سندرم افتالمپلژی (اختلال)"@fa, "Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder)"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/240086009> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/240086009> .

ns0:Finding_site rdfs:label "محل یافتن"@fa, "Finding site"@en .
<http://www.irandoc.acir/onto/irandoc/703544004>
  skos:prefLabel "انحطاط نورون حرکتی تحتانی با بیماری استخوانی مانند پاژه"@fa, "Lower motor neuron degeneration with Paget-like bone disease"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  ns0:Is_a <http://www.irandoc.acir/onto/irandoc/240086009> ;
  skos:broader <http://www.irandoc.acir/onto/irandoc/240086009> .

<http://www.irandoc.acir/onto/irandoc/89886004>
  skos:prefLabel "ناهنجاری مادرزادی عضله اسکلتی"@fa, "Congenital anomaly of skeletal muscle"@en ;
  a <http://www.irandoc.ac.ir/onto/irandoc-meta/Concept>, skos:Concept ;
  skos:narrower <http://www.irandoc.acir/onto/irandoc/240086009> .

ns0:Pathological_process rdfs:label "فرآیند پاتولوژیک"@fa, "Pathological process"@en .