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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000117"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000119"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    


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    <!-- http://purl.obolibrary.org/obo/BCGO_0000002 -->

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        <rdfs:label xml:lang="en">mouse strain</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/BCGO_9001261 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/BCGO_9001261">
        <rdfs:label xml:lang="en">NOD.Cg-Rag1{tm1Mom}Ins2{Akita}Il2rg{tm1Wjl}/Sz mouse strain</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/BCGO_0000002"/>
        <ns2:IAO_0000115 xml:lang="en">A mouse strain in which the targeted gene, recombination activating gene 1 (NCBI Gene ID: 19373), has been modified (allele type: Global Null) to  (MGI ID: Rag1{tm1Mom}). Backcrossing of the Rag1 null allele onto the NOD/Lt strain background (NOD-Rag1{null} mice) provided a radio-resistant and longer-lived model for human-cell engraftment. Mutations in X-chromosome-linked Il2rg gene cause X-linked severe combined immunodeficiency (XSCID). Immunodeficient NOD-Rag1{null} IL2rg nullmice tolerated much higher levels of irradiation conditioning than did NOD-Prkdcscid IL2rg{null} mice. This immunodeficient mouse also develops spontaneous hyperglycemia based on the Ins2{Akita} mutation.</ns2:IAO_0000115>
        <ns2:IAO_0000118 xml:lang="en">NOD.Cg-Rag1{tm1Mom}Ins2{Akita}Il2rg{tm1Wjl}/Sz</ns2:IAO_0000118>
        <ns2:IAO_0000117 xml:lang="en">Person: Mark A. Magnuson, Jill Lindner, Jean-Philippe Cartailler</ns2:IAO_0000117>
        <ns2:IAO_0000119 xml:lang="en">Vanderbilt University Medical Center</ns2:IAO_0000119>
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