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    <!-- http://purl.obolibrary.org/obo/MP_0000955 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MP_0000955">
        <rdfs:label>abnormal spinal cord morphology</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MP_0005297 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MP_0005297">
        <rdfs:label>spina bifida occulta</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MP_0012710 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MP_0012710">
        <rdfs:label>diastematomyelia</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MP_0000955"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MP_0005297"/>
        <oboInOwl:hasExactSynonym>diastomyelia</oboInOwl:hasExactSynonym>
        <oboInOwl:created_by>csmith</oboInOwl:created_by>
        <oboInOwl:creation_date>2014-03-20T14:10:17Z</oboInOwl:creation_date>
        <ns4:IAO_0000115>a rare congenital anomaly that results in the splitting of the spinal cord in a longitudinal direction, usually at the level of the upper lumbar vertebra; this condition occurs in the presence of an osseous (bone), cartilaginous or fibrous septum in the central portion of the spinal canal which then produces a complete or incomplete sagittal division of the spinal cord into two hemicords, each half being surrounded by a dural sac; when the split does not reunite distally to the spur, the condition is referred to as a diplomyelia</ns4:IAO_0000115>
        <oboInOwl:id>MP:0012710</oboInOwl:id>
        <oboInOwl:hasOBONamespace>MPheno.ontology</oboInOwl:hasOBONamespace>
        <dcterms:contributor rdf:resource="https://orcid.org/0000-0003-3691-0324"/>
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    <!-- http://purl.obolibrary.org/obo/NCBITaxon_9606 -->

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