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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000117"/>
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    <!-- http://purl.obolibrary.org/obo/DOID_0050177 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_0050177">
        <rdfs:label>simple genetic disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/DOID_1307 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_1307">
        <rdfs:label>dementia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/DOID_679 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_679">
        <rdfs:label>basal ganglia disease</rdfs:label>
    </Class>
    


    <!-- http://www.ebi.ac.uk/efo/EFO_0000533 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0000533">
        <rdfs:label>Huntington&#39;s disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_0050177"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_1307"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_679"/>
        <ns2:IAO_0000119>GeneRIF:15057517</ns2:IAO_0000119>
        <ns2:IAO_0000118>HD - Huntington chorea</ns2:IAO_0000118>
        <ns2:IAO_0000118>Huntington Disease, Juvenile-Onset</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12078510</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:14751289</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12950446</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12969257</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:16054230</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12952868</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:14511117</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12008025</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11593450</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:14522959</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12736330</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12657678</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15922606</ns2:IAO_0000119>
        <ns2:IAO_0000117>James Malone</ns2:IAO_0000117>
        <ns2:IAO_0000118>Huntington disease</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:14985389</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:14725621</ns2:IAO_0000119>
        <ns2:IAO_0000118>HUNTINGTON&#39;S CHOREA</ns2:IAO_0000118>
        <ns2:IAO_0000118>Huntington Disease, Akinetic Rigid Variant</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15843398</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15033177</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15742215</ns2:IAO_0000119>
        <ns2:IAO_0000118>Huntington&#39;s</ns2:IAO_0000118>
        <rdfs:seeAlso>URI: http://www.ebi.ac.uk/cellline#Huntington&#39;s_disease</rdfs:seeAlso>
        <ns2:IAO_0000119>GeneRIF:11817536</ns2:IAO_0000119>
        <ns2:IAO_0000118>LATE ONSET HUNTINGTON DIS</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12528814</ns2:IAO_0000119>
        <ns2:IAO_0000118>Huntington&#39;s chorea (disorder)</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:11813242</ns2:IAO_0000119>
        <ns2:IAO_0000118>HD</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15476444</ns2:IAO_0000119>
        <ns2:IAO_0000118>JUVENILE HUNTINGTON DIS</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12682342</ns2:IAO_0000119>
        <rdfs:comment>A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4)</rdfs:comment>
        <rdfs:comment>A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea.</rdfs:comment>
        <ns2:IAO_0000119>GeneRIF:12614934</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15644269</ns2:IAO_0000119>
        <ns2:IAO_0000118>HC - Huntington chorea</ns2:IAO_0000118>
        <ns2:IAO_0000118>HUNTINGTON DIS AKINETIC RIGID VARIANT</ns2:IAO_0000118>
        <ns2:IAO_0000119>SNOMEDCT:58756001</ns2:IAO_0000119>
        <ns2:IAO_0000118>Chronic Progressive Hereditary Chorea (Huntington)</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15359012</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12915485</ns2:IAO_0000119>
        <ns2:IAO_0000119>ICD9:333.4</ns2:IAO_0000119>
        <ns2:IAO_0000118>Chronic progressive chorea</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12691731</ns2:IAO_0000119>
        <ns2:IAO_0000118>Chorea, Huntington</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15878807</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12706247</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12781994</ns2:IAO_0000119>
        <ns2:IAO_0000118>JUVENILE ONSET HUNTINGTON DIS</ns2:IAO_0000118>
        <ns2:IAO_0000118>HUNTINGTON DIS</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15749339</ns2:IAO_0000119>
        <ns2:IAO_0000119>MSH:D006816</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15261377</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12890790</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11914418</ns2:IAO_0000119>
        <ns2:IAO_0000118>Juvenile Huntington Disease</ns2:IAO_0000118>
        <ns2:IAO_0000119>NIFSTD:birnlex_12500</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12531510</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12604778</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:16184606</ns2:IAO_0000119>
        <ns2:IAO_0000119>DOID:12858</ns2:IAO_0000119>
        <ns2:IAO_0000118>Huntington&#39;s disease</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15817265</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15337316</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15934928</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15845076</ns2:IAO_0000119>
        <ns2:IAO_0000118>Huntington&#39;s disease pathway</ns2:IAO_0000118>
        <ns2:IAO_0000118>Huntington Disease, Late Onset</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:11432963</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15383276</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15715085</ns2:IAO_0000119>
        <ns2:IAO_0000118>Chronic progressive hereditary chorea</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15496672</ns2:IAO_0000119>
        <ns2:IAO_0000118>Akinetic Rigid Variant of Huntington Disease</ns2:IAO_0000118>
        <ns2:IAO_0000117>Tomasz Adamusiak</ns2:IAO_0000117>
        <ns2:IAO_0000119>GeneRIF:12960759</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15009635</ns2:IAO_0000119>
        <ns2:IAO_0000118>HUNTINGTONS DIS</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:14981075</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15880743</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:14978262</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15029481</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:16115812</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15167689</ns2:IAO_0000119>
    </Class>
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