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DESCRIBE <http://purl.uniprot.org/SHA-384/1518C9726AC2EF240BDAB6409BB6845E56C99C5AAB057B0800AB429B610ADC517554DBA5CD0C6A51A71213F2FEF55B8E>
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http://purl.uniprot.org/SHA-384/1518C9726AC2EF240BDAB6409BB6845E56C99C5AAB057B0800AB429B610ADC517554DBA5CD0C6A51A71213F2FEF55B8E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/1518C9726AC2EF240BDAB6409BB6845E56C99C5AAB057B0800AB429B610ADC517554DBA5CD0C6A51A71213F2FEF55B8E
http://www.w3.org/2000/01/rdf-schema#comment
"Murine models of congenital central hypoventilation syndrome designed with PHOX2B mutations have suggested RTN neuron agenesis."
xsd:string
http://purl.uniprot.org/uniprot/#_458D61A180E4E341D30443099456A26B15E737BAC6805EA1288081A9BD16D023FE21569113A812951BB1E8CB62860760
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/1518C9726AC2EF240BDAB6409BB6845E56C99C5AAB057B0800AB429B610ADC517554DBA5CD0C6A51A71213F2FEF55B8E
http://purl.uniprot.org/uniprot/Q8C741
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1518C9726AC2EF240BDAB6409BB6845E56C99C5AAB057B0800AB429B610ADC517554DBA5CD0C6A51A71213F2FEF55B8E
http://purl.uniprot.org/uniprot/#_Q8C741-mappedCitation-27226447
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1518C9726AC2EF240BDAB6409BB6845E56C99C5AAB057B0800AB429B610ADC517554DBA5CD0C6A51A71213F2FEF55B8E