<?xml version="1.0"?>
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     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
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     xmlns:ns3="http://edamontology.org/">
    


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    <AnnotationProperty rdf:about="http://edamontology.org/created_in"/>
    <AnnotationProperty rdf:about="http://edamontology.org/operations"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://edamontology.org/bio"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
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    <!-- http://edamontology.org/operation_0484 -->

    <Class rdf:about="http://edamontology.org/operation_0484">
        <rdfs:label>SNP detection</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://edamontology.org/operation_3227"/>
        <rdfs:comment>This includes functional SNPs for large-scale genotyping purposes, disease-associated non-synonymous SNPs etc.</rdfs:comment>
        <oboInOwl:hasExactSynonym>SNP discovery</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>SNP calling</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Single nucleotide polymorphism detection</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDefinition>Find single nucleotide polymorphisms (SNPs) - single nucleotide change in base positions - between sequences. Typically done for sequences from a high-throughput sequencing experiment that differ from a reference genome and which might, especially by reference to population frequency or functional data, indicate a polymorphism.</oboInOwl:hasDefinition>
        <ns3:created_in>beta12orEarlier</ns3:created_in>
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    <!-- http://edamontology.org/operation_3227 -->

    <Class rdf:about="http://edamontology.org/operation_3227">
        <rdfs:label>Variant calling</rdfs:label>
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