<?xml version="1.0"?>
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     xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
     xmlns:owl="http://www.w3.org/2002/07/owl#"
     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
     xmlns:xsd="http://www.w3.org/2001/XMLSchema#"
     xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#"
     xmlns:ns4="http://edamontology.org/"
     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
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    //
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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"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDefinition"/>
    


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    <!-- http://edamontology.org/has_output -->

    <ObjectProperty rdf:about="http://edamontology.org/has_output">
        <rdfs:label>has output</rdfs:label>
    </ObjectProperty>
    


    <!-- 
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    <!-- http://edamontology.org/data_1863 -->

    <Class rdf:about="http://edamontology.org/data_1863">
        <rdfs:label>Haplotype map</rdfs:label>
    </Class>
    


    <!-- http://edamontology.org/operation_0282 -->

    <Class rdf:about="http://edamontology.org/operation_0282">
        <rdfs:label>Genetic mapping</rdfs:label>
    </Class>
    


    <!-- http://edamontology.org/operation_0487 -->

    <Class rdf:about="http://edamontology.org/operation_0487">
        <rdfs:label>Haplotype mapping</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://edamontology.org/operation_0282"/>
        <rdfs:subClassOf>
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                <someValuesFrom rdf:resource="http://edamontology.org/data_1863"/>
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        <oboInOwl:hasExactSynonym>Haplotype reconstruction</oboInOwl:hasExactSynonym>
        <ns4:created_in>beta12orEarlier</ns4:created_in>
        <oboInOwl:hasExactSynonym>Haplotype map generation</oboInOwl:hasExactSynonym>
        <rdfs:comment>Haplotype inference can help in population genetic studies and the identification of complex disease genes, , and is typically based on aligned single nucleotide polymorphism (SNP) fragments. Haplotype comparison is a useful way to characterize the genetic variation between individuals. An individual&#39;s haplotype describes which nucleotide base occurs at each position for a set of common SNPs. Tools might use combinatorial functions (for example parsimony) or a likelihood function or model with optimisation such as minimum error correction (MEC) model, expectation-maximisation algorithm (EM), genetic algorithm or Markov chain Monte Carlo (MCMC).</rdfs:comment>
        <oboInOwl:hasExactSynonym>Haplotype inference</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDefinition>Infer haplotypes, either alleles at multiple loci that are transmitted together on the same chromosome, or a set of single nucleotide polymorphisms (SNPs) on a single chromatid that are statistically associated.</oboInOwl:hasDefinition>
        <oboInOwl:inSubset rdf:resource="http://edamontology.org/bio"/>
        <oboInOwl:inSubset rdf:resource="http://edamontology.org/operations"/>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



