<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/PCL?iri=http://purl.obolibrary.org/obo/PCL_0016455"?>
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     xmlns:owl="http://www.w3.org/2002/07/owl#"
     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
     xmlns:pcl="http://purl.obolibrary.org/obo/pcl/"
     xmlns:xsd="http://www.w3.org/2001/XMLSchema#"
     xmlns:skos="http://www.w3.org/2004/02/skos/core#"
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    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Annotation properties
    //
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/PCL_0010061"/>
    <AnnotationProperty rdf:about="http://schema.org/assesses"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#prefLabel"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000028"/>
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    <AnnotationProperty rdf:about="http://schema.org/archivedAt"/>
    <AnnotationProperty rdf:about="http://schema.org/position"/>
    <AnnotationProperty rdf:about="http://schema.org/discussionUrl"/>
    


    <!-- 
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    <!-- 
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    //
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    <!-- http://purl.obolibrary.org/obo/PCL_0010002 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/PCL_0010002"/>
    


    <!-- http://schema.org/Dataset -->

    <Class rdf:about="http://schema.org/Dataset"/>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Individuals
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    <!-- http://purl.obolibrary.org/obo/PCL_0016455 -->

    <NamedIndividual rdf:about="http://purl.obolibrary.org/obo/PCL_0016455">
        <rdf:type rdf:resource="http://schema.org/Dataset"/>
        <rdfs:label>Human M1 (CCN201912131) single nuclei snmC-Seq2</rdfs:label>
        <ns2:PCL_0010061 rdf:datatype="http://www.w3.org/2001/XMLSchema#integer">5222</ns2:PCL_0010061>
        <ns2:IAO_0000028>Human M1 snmC-Seq2</ns2:IAO_0000028>
        <ns3:position>M1</ns3:position>
        <ns3:archivedAt>https://knowledge.brain-map.org/data/WX7CGKE3I2ILINMFSHD/summary</ns3:archivedAt>
        <rdfs:comment>A single-nucleus sequencing assay (library preparation method) that involves fragmentation of genomic DNA followed by adapter ligation, bisulfite conversion and limited amplification using adapter-specific PCR primers in preparation for sequencing. This enables the genome-wide indentification of cytosine DNA methylation states at single-base resolution. </rdfs:comment>
        <skos:prefLabel>snmC-Seq2</skos:prefLabel>
        <ns3:discussionUrl>https://nemoanalytics.org//index.html?layout_id=ac9863bf</ns3:discussionUrl>
        <ns3:assesses>human</ns3:assesses>
        <ns3:includedInDataCatalog rdf:resource="http://purl.obolibrary.org/obo/pcl/CCN201912131"/>
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    <!-- http://purl.obolibrary.org/obo/pcl/CCN201912131 -->

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        <rdf:type rdf:resource="http://purl.obolibrary.org/obo/PCL_0010002"/>
        <rdfs:label>CCN201912131</rdfs:label>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



