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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000118"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    


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    <!-- http://purl.obolibrary.org/obo/BFO_0000117 -->

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        <rdfs:label xml:lang="en">has occurrent part</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/RO_0000057 -->

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        <rdfs:label xml:lang="en">has participant</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/BFO_0000040 -->

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        <rdfs:label xml:lang="en">material entity</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/DIDEO_00000020 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DIDEO_00000020">
        <rdfs:label xml:lang="en">drug-drug interaction</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/GO_0008150"/>
        <rdfs:subClassOf>
            <Restriction>
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        <ns3:IAO_0000115 xml:lang="en">A biological process that results in a clinically meaningful change to the response of at least one co-administrated drug.</ns3:IAO_0000115>
        <rdfs:comment xml:lang="en">A clinically meaningful alteration in the exposure and/or response to a drug (object drug) that has occurred as a result of the co-administration of another drug (precipitant drug)Oates JA. Chapter 5. Goodman and Gilman 11th ed (2006):117–36; Hines. Response can refer to either precipitating an adverse event or altering the therapeutic effect of the object drug. Although some DDIs may be used for therapeutic benefit, this paper focuses on those with adverse clinical consequences. (based on the 2013 DDI conference series) / has participant some mechanism.</rdfs:comment>
        <ns3:IAO_0000118 xml:lang="en">DDI</ns3:IAO_0000118>
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    <!-- http://purl.obolibrary.org/obo/DIDEO_00000021 -->

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        <rdfs:label xml:lang="en">drug co-administration</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/GO_0008150 -->

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        <rdfs:label>biological_process</rdfs:label>
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