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        <rdfs:label xml:lang="en">has part</rdfs:label>
        <rdfs:label>has_part</rdfs:label>
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    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/BFO_0000112">
        <rdfs:label xml:lang="en">has disposition at some time</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/IDO_0100879 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/IDO_0100879">
        <rdfs:label xml:lang="en">attenuated disposition</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/IDO_0101057 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/IDO_0101057">
        <rdfs:label xml:lang="en">B. suis hisF mutant</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/IDO_0110379 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/IDO_0110379">
        <rdfs:label>B. abortus 2308 hisF mutant</rdfs:label>
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        <rdfs:seeAlso>UniProtKB accession: Q2YQY8</rdfs:seeAlso>
        <rdfs:comment>Information about the mutated molecule: FUNCTION: IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The hisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the hisH subunit (By similarity)(Swiss-Prot: Q8FY07).  CATALYTIC ACTIVITY: 5-[(5-phospho-1-deoxyribulos-1-ylamino)methylideneamino]-1-(5-phosphoribosyl)imidazole-4-carboxamide + L-glutamine = imidazole-glycerol phosphate + 5-aminoimidazol-4-carboxamide ribonucleotide + L-glutamate + H(2)O(Swiss-Prot: Q8FY07).  PATHWAY: Amino-acid biosynthesis</rdfs:comment>
        <ns3:IAO_0000115>A mutant of strain Brucella melitensis biovar Abortus 2308 that lacks an intact gene hisF.</ns3:IAO_0000115>
        <ns3:IAO_0000117>YH</ns3:IAO_0000117>
        <ns3:IAO_0000119>PMID: L-histidine biosynthesis</ns3:IAO_0000119>
        <rdfs:seeAlso>NCBIGene: 3788754</rdfs:seeAlso>
        <rdfs:comment>The gene hisF from the strain Brucella melitensis biovar Abortus 2308 is a virulence gene.</rdfs:comment>
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