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_:vb50943284	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with a missing Nexin link, infantile onset of chronic sinopulmonary infections, and has_material_basis_in homozygous mutation in the DRC1 gene on chromosome 2p23."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50943284	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://www.ncbi.nlm.nih.gov/pubmed/26998415"^^<http://www.w3.org/2001/XMLSchema#string> .
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_:vb50943284	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
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_:vb50943284	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .