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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000117"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0004822 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0004822">
        <rdfs:label>bronchiectasis</rdfs:label>
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    <!-- http://www.ebi.ac.uk/efo/EFO_0920041 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0920041">
        <rdfs:label xml:lang="en">heritable connective tissue disorder-associated bronchiectasis</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0004822"/>
        <oboInOwl:hasExactSynonym>connective tissue-predominant bronchiectasis</oboInOwl:hasExactSynonym>
        <rdfs:seeAlso>https://github.com/EBISPOT/efo/issues/2546</rdfs:seeAlso>
        <oboInOwl:hasRelatedSynonym>Marfan-like bronchiectasis</oboInOwl:hasRelatedSynonym>
        <ns2:IAO_0000117>AI agent</ns2:IAO_0000117>
        <ns2:IAO_0000115>A bronchiectasis endotype associated with heritable connective tissue disorder features, characterized by a tall asthenic morphotype with high rates of scoliosis, pectus excavatum, mitral valve prolapse, and dural ectasia. This endotype is associated with susceptibility to pulmonary nontuberculous mycobacterial infection and may involve genetic variation in connective tissue and transforming growth factor-beta (TGF-beta)-related pathway genes.</ns2:IAO_0000115>
        <oboInOwl:hasNarrowSynonym>Lady Windermere syndrome</oboInOwl:hasNarrowSynonym>
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