<http://purl.obolibrary.org/obo/DOID_0110625>	<http://www.w3.org/2000/01/rdf-schema#label>	"primary ciliary dyskinesia 20"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110625>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"primary ciliary dyskinesia 20 with or without situs inversus"@en .
<http://purl.obolibrary.org/obo/DOID_0110625>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"CILD20"@en .
<http://purl.obolibrary.org/obo/DOID_0110625>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110625"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110625>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_0110625>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, infantile onset of chronic sinopulmonary infections, and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the CCDC114 gene on chromosome 19q13."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110625>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_9562> .
<http://purl.obolibrary.org/obo/DOID_0110625>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q34.8"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110625>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110625>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0110625>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:615067"^^<http://www.w3.org/2001/XMLSchema#string> .