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    <!-- http://purl.obolibrary.org/obo/ECO_0000015 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/ECO_0000015">
        <rdfs:label>mutant phenotype evidence</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/ECO_0001038 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/ECO_0001038">
        <rdfs:label>deletion mutation phenotypic evidence</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/ECO_0000015"/>
        <oboInOwl:hasAlternativeId>ECO:0005510</oboInOwl:hasAlternativeId>
        <oboInOwl:id>ECO:0001038</oboInOwl:id>
        <ns2:IAO_0000112>In contrast, and in full agreement with the previous results of Wade et al. (17), the longer deletion in the TB23 fragment, that removes MelR binding site 2, results in a sharp reduction in the repression of the melR promoter by MelR.</ns2:IAO_0000112>
        <rdfs:comment>The length of the DNA deleted can range from a single nucleotide to enough material that could include multiple genes.</rdfs:comment>
        <oboInOwl:hasOBONamespace>eco</oboInOwl:hasOBONamespace>
        <rdfs:comment>As a child of &#39;experimental phenotypic evidence&#39;, this is not to be confused with the biological processes deletion mutation / deletion deficiency in which DNA is lost during DNA replication.</rdfs:comment>
        <rdfs:comment>Contrast with knockout phenotypic evidence in which any number of changes to the DNA result in elimination of the function of the gene in question.</rdfs:comment>
        <oboInOwl:created_by>mchibucos</oboInOwl:created_by>
        <ns2:IAO_0000234>SIB:PG</ns2:IAO_0000234>
        <oboInOwl:creation_date>2014-03-16T11:30:54Z</oboInOwl:creation_date>
        <ns2:IAO_0000115>A type of mutant phenotype evidence resulting from a mutation in which there is the removal of one or more contiguous nucleotides that may result in altered function or other measurable properties.</ns2:IAO_0000115>
        <oboInOwl:hasExactSynonym>deletion mutation evidence</oboInOwl:hasExactSynonym>
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