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        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts (MeSH).</rdfs:comment>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)</rdfs:comment>
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        <ns3:IAO_0000118 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Guam Form of Amyotrophic Lateral Sclerosis</ns3:IAO_0000118>
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        <ns3:IAO_0000117 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">James Malone</ns3:IAO_0000117>
        <ns3:IAO_0000118 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">LOU GEHRIG DIS</ns3:IAO_0000118>
        <ns3:IAO_0000118 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">LOU GEHRIGS DIS</ns3:IAO_0000118>
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        <ns3:IAO_0000118 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">MOTOR NEURON DIS AMYOTROPHIC LATERAL SCLEROSIS</ns3:IAO_0000118>
        <ns3:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">MSH:D000690</ns3:IAO_0000119>
        <ns3:IAO_0000118 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Motor Neuron Disease, Amyotrophic Lateral Sclerosis</ns3:IAO_0000118>
        <ns3:IAO_0000118 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Motor neuron disease, bulbar</ns3:IAO_0000118>
        <ns3:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">NCIt:C34373</ns3:IAO_0000119>
        <ns3:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">NIFSTD:birnlex_12566</ns3:IAO_0000119>
        <ns3:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">SNOMEDCT:86044005</ns3:IAO_0000119>
        <ns3:IAO_0000117 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Tomasz Adamusiak</ns3:IAO_0000117>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#string">URI: http://www.ebi.ac.uk/cellline#amyotrophic_lateral_sclerosis</rdfs:seeAlso>
        <ns3:IAO_0000118 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">amyotrophic lateral sclerosis</ns3:IAO_0000118>
        <ns3:IAO_0000412 rdf:resource="http://purl.obolibrary.org/obo/clo.owl"/>
    </Class>
    


    <!-- http://www.ebi.ac.uk/efo/EFO_0000908 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0000908">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">central nervous system</rdfs:label>
    </Class>
</rdf:RDF>



<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



