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    <!-- http://purl.obolibrary.org/obo/RO_0002233 -->

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    <!-- http://purl.obolibrary.org/obo/HINO_0004585 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HINO_0004585">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ligands of SLC29A3</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HINO_0004587 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ligands of SLC29A3</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HINO_0010099 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HINO_0010099">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Equilibrative transport (import) of nucleosides and adenine by solute carrier family 29 (nucleoside transporters), member 3</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/INO_0000040"/>
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        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Authored: Jassal, B, 2010-05-12</rdfs:comment>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Edited: Jassal, B, 2010-05-12</rdfs:comment>
        <ns3:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Pubmed15701636</ns3:IAO_0000119>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Reactome Database ID Release 43727767</rdfs:seeAlso>
        <ns3:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Reactome, http://www.reactome.org</ns3:IAO_0000119>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ReactomeREACT_22395</rdfs:seeAlso>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Reviewed: He, L, 2010-05-10</rdfs:comment>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">The human gene SLC29A3 encodes the equilibrative nucleoside transporter 3 (ENT3). It is abundant in many tissues, especially the placenta and is localized intracellularly on the lysosomal membrane. ENT3 mediates the reversible transport of nucleosides and the nucleobase adenine (Baldwin SA et al, 2005). Defects in SLC29A3 are the cause of H syndrome, an autosomal recessive disorder(Molho-Pessach V et al, 2008).</rdfs:comment>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/INO_0000040 -->

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