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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_26 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_26">
        <rdfs:label>pancreas disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/DOID_850 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_850">
        <rdfs:label>lung disease</rdfs:label>
    </Class>
    


    <!-- http://www.ebi.ac.uk/efo/EFO_0000390 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0000390">
        <rdfs:label>cystic fibrosis</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_0050177"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_26"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_850"/>
        <ns2:IAO_0000119>GeneRIF:15611333</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12026214</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15107292</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15738290</ns2:IAO_0000119>
        <ns2:IAO_0000118>cystic fibrosis with pulmonary manifestations</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12070134</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12820707</ns2:IAO_0000119>
        <ns2:IAO_0000118>Cystic fibrosis NOS</ns2:IAO_0000118>
        <ns2:IAO_0000118>Meconium ileus in cystic fibrosis (disorder)</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:11872746</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15025720</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15537723</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11877474</ns2:IAO_0000119>
        <ns2:IAO_0000119>SNOMEDCT:190905008</ns2:IAO_0000119>
        <ns2:IAO_0000119>NCIt:C2975</ns2:IAO_0000119>
        <ns2:IAO_0000117>James Malone</ns2:IAO_0000117>
        <ns2:IAO_0000119>GeneRIF:16137181</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12547728</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12151438</ns2:IAO_0000119>
        <ns2:IAO_0000118>Meconium obstruction of intestine in mucoviscidosis</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12142723</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12142724</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15025858</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15533353</ns2:IAO_0000119>
        <ns2:IAO_0000119>SNOMEDCT:190911006</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12660625</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12297838</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15246975</ns2:IAO_0000119>
        <ns2:IAO_0000118>cystic fibrosis</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:11845300</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12579467</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:14685937</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:14699484</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11984593</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15463896</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15463895</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15463893</ns2:IAO_0000119>
        <ns2:IAO_0000118>Cystic fibrosis (disorder)</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15490240</ns2:IAO_0000119>
        <ns2:IAO_0000118>cystic fibrosis with gastrointestinal manifestations</ns2:IAO_0000118>
        <ns2:IAO_0000118>cystic fibrosis with other manifestations</ns2:IAO_0000118>
        <ns2:IAO_0000118>Mucoviscidosis</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15579374</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12220181</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12732620</ns2:IAO_0000119>
        <ns2:IAO_0000118>CYSTIC FIBROS W/O ILEUS</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12000722</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15274124</ns2:IAO_0000119>
        <ns2:IAO_0000118>CF - Cystic fibrosis</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:16207846</ns2:IAO_0000119>
        <ns2:IAO_0000118>Cystic fibrosis NOS (disorder)</ns2:IAO_0000118>
        <ns2:IAO_0000118>cystic fibrosis with combined manifestations</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15964894</ns2:IAO_0000119>
        <ns2:IAO_0000118>Fibrocystic disease</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:15781764</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15024729</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15964250</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15184199</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15489228</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11667971</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15385508</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15684701</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15367919</ns2:IAO_0000119>
        <ns2:IAO_0000118>CF</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:16267280</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:16236890</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12692180</ns2:IAO_0000119>
        <ns2:IAO_0000119>ICD9:277.00</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12847263</ns2:IAO_0000119>
        <ns2:IAO_0000119>DOID:1485</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11956211</ns2:IAO_0000119>
        <ns2:IAO_0000119>ICD9:277.0</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15336594</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11823525</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15007059</ns2:IAO_0000119>
        <rdfs:comment>A congenital metabolic disorder affecting the exocrine glands, inherited as an autosomal trait. The secretions of exocrine glands are abnormal, resulting in excessively viscid mucus production which causes obstruction of passageways (including pancreatic and bile ducts, intestines, and bronchi). The sweat sodium and chloride content are increased. Symptoms usually appear in childhood and include meconium ileus, poor growth despite good appetite, malabsorption and foul bulky stools, chronic bronchitis with cough, recurrent pneumonia, bronchiectasis, emphysema, clubbing of the fingers, and salt depletion in hot weather.</rdfs:comment>
        <ns2:IAO_0000118>cystic fibrosis with meconium ileus (disorder)</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:11988083</ns2:IAO_0000119>
        <ns2:IAO_0000118>cystic fibrosis with pulmonary manifestations (disorder)</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:14695120</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15070876</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12919146</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15638824</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11809765</ns2:IAO_0000119>
        <rdfs:seeAlso>URI: http://www.ebi.ac.uk/cellline#cystic_fibrosis</rdfs:seeAlso>
        <ns2:IAO_0000119>GeneRIF:12370389</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12948935</ns2:IAO_0000119>
        <ns2:IAO_0000118>cystic fibrosis with meconium ileus</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:16281647</ns2:IAO_0000119>
        <rdfs:comment>A congenital metabolic disorder affecting the exocrine glands, inherited as an autosomal trait. The secretions of exocrine glands are abnormal, resulting in excessively viscid mucus production which causes obstruction of passageways (including pancreatic and bile ducts, intestines, and bronchi).  The sweat sodium and chloride content are increased.  Symptoms usually appear in childhood and include meconium ileus, poor growth despite good appetite, malabsorption and foul bulky stools, chronic bronchitis with cough, recurrent pneumonia, bronchiectasis, emphysema, clubbing of the fingers, and salt depletion in hot weather. -- 2003</rdfs:comment>
        <ns2:IAO_0000118>Cystic fibrosis without mention of meconium ileus</ns2:IAO_0000118>
        <ns2:IAO_0000118>cystic fibrosis with other manifestations (disorder)</ns2:IAO_0000118>
    </Class>
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