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    <!-- http://purl.obolibrary.org/obo/HINO_0005150 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">PathwayStep2058</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HINO_0005185 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">PathwayStep2065</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HINO_0014537 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HINO_0014537">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Incretin Synthesis, Secretion, and Inactivation</rdfs:label>
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        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Authored: May, B, 2009-05-18 21:31:59</rdfs:comment>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Edited: May, B, 2009-05-18 21:31:59</rdfs:comment>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#string">GENE ONTOLOGYGO:0050796</rdfs:seeAlso>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Incretins are peptide hormones produced by the gut that enhance the ability of glucose to stimulate insulin secretion from beta cells in the pancreas. Two incretins have been identified: Glucagon-like Peptide-1 (GLP-1) and Glucose-dependent Insulinotropic Polypeptide (GIP, initially named Gastric Inhibitory Peptide). Both are released by cells of the small intestine, GLP-1 from L cells and GIP from K cells.&lt;br&gt;The control of incretin secretion is complex. Fatty acids, phospholipids, glucose, acetylcholine, leptin, and Gastrin-releasing Peptide all stimulate secretion of GLP-1. Fatty acids and phospholipids are the primary stimulants of secretion of GIP in humans (carbohydrates have more effect in rodents).&lt;br&gt;Incretins secreted into the bloodstream are subject to rapid inactivation by Dipeptidyl Peptidase IV (DPP IV), which confers half-lives of only a few minutes onto GLP-1 and GIP. Inhibitors of DPP IV, for example sitagliptin, are now being used in the treatment of Type 2 diabetes.</rdfs:comment>
        <ns3:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Pubmed17263764</ns3:IAO_0000119>
        <ns3:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Pubmed17498508</ns3:IAO_0000119>
        <ns3:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Pubmed19074620</ns3:IAO_0000119>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Reactome Database ID Release 43400508</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_23974</rdfs:seeAlso>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Reviewed: Bloom, SR, 2010-06-24</rdfs:comment>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HINO_0014553 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HINO_0014553">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Synthesis, Secretion, and Inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP)</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HINO_0014555 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Synthesis, Secretion, and Inactivation of Glucagon-like Peptide-1 (GLP-1)</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/INO_0000021 -->

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    <!-- http://purl.obolibrary.org/obo/NCBITaxon_9606 -->

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