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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/HP_0011627 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0011627">
        <rdfs:label>Aorto-ventricular tunnel</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0031932 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0031932">
        <rdfs:label>Aorto-left ventricular tunnel</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0011627"/>
        <dcterms:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2018-07-04T20:38:35Z</dcterms:date>
        <rdfs:comment>ALVT is extremely rare with incidence as low as 0.001% of all congenital heart diseases. Most of the patients develop symptoms of heart failure during the first year of life. The onset, severity and progression of heart failure vary and ranges from in-utero fetal death to asymptomatic adulthood.</rdfs:comment>
        <ns3:IAO_0000115>Aorto-left ventricular tunnel (ALVT) is a congenital extracardiac channel connecting the ascending aorta above the sino-tubular junction to either left or right ventricular cavity.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>Left ventricle to aorta tunnel</oboInOwl:hasExactSynonym>
        <dcterms:creator rdf:resource="https://orcid.org/0000-0002-0736-9199"/>
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