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DESCRIBE <http://purl.uniprot.org/SHA-384/03EF36427628D900F8399FDD6307D201F45A2EFD3E6CE049F0875DEFF02577EED6E142D2D0A5859855A40C59E5B76CE9>
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http://purl.uniprot.org/SHA-384/03EF36427628D900F8399FDD6307D201F45A2EFD3E6CE049F0875DEFF02577EED6E142D2D0A5859855A40C59E5B76CE9
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/03EF36427628D900F8399FDD6307D201F45A2EFD3E6CE049F0875DEFF02577EED6E142D2D0A5859855A40C59E5B76CE9
http://www.w3.org/2000/01/rdf-schema#comment
"The mutational testing found a heterozygous deletion in NRXN1 in one patient."
xsd:string
http://purl.uniprot.org/uniprot/#_ECB6C983B923CACB8E44E44AA9752187FB987A54E71554FE43AAE7976686B699F1EB56A3A8A804A5E0F6D2E1C24DDE3C
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/03EF36427628D900F8399FDD6307D201F45A2EFD3E6CE049F0875DEFF02577EED6E142D2D0A5859855A40C59E5B76CE9
http://purl.uniprot.org/uniprot/A0A0D9SEQ7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/03EF36427628D900F8399FDD6307D201F45A2EFD3E6CE049F0875DEFF02577EED6E142D2D0A5859855A40C59E5B76CE9
http://purl.uniprot.org/uniprot/#_A0A0D9SEQ7-mappedCitation-21827697
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/03EF36427628D900F8399FDD6307D201F45A2EFD3E6CE049F0875DEFF02577EED6E142D2D0A5859855A40C59E5B76CE9