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DESCRIBE <http://purl.uniprot.org/SHA-384/EDB7BC295374BFC70DCA738C0C4AED7CBC4EFF7D5DED08AD8E0BEE35B6F73E7592D652ADBF5310218B790501F6657B51>
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http://purl.uniprot.org/SHA-384/EDB7BC295374BFC70DCA738C0C4AED7CBC4EFF7D5DED08AD8E0BEE35B6F73E7592D652ADBF5310218B790501F6657B51
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/EDB7BC295374BFC70DCA738C0C4AED7CBC4EFF7D5DED08AD8E0BEE35B6F73E7592D652ADBF5310218B790501F6657B51
http://www.w3.org/2000/01/rdf-schema#comment
"XPO1 and OXT1 may contribute to ASD in 2p15-p16.1 deletion cases and non-deletion cases of ASD mapping to this chromosome region."
xsd:string
http://purl.uniprot.org/uniprot/#_F507526B8D3EADBC2E855B4E508F5F3E749E6EA046BCF416CCB04BF4C9894B1D20C099B45A4929F0E52684BCF60AC3FC
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/EDB7BC295374BFC70DCA738C0C4AED7CBC4EFF7D5DED08AD8E0BEE35B6F73E7592D652ADBF5310218B790501F6657B51
http://purl.uniprot.org/uniprot/A0A7I2V2Y6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EDB7BC295374BFC70DCA738C0C4AED7CBC4EFF7D5DED08AD8E0BEE35B6F73E7592D652ADBF5310218B790501F6657B51
http://purl.uniprot.org/uniprot/#_A0A7I2V2Y6-mappedCitation-21750575
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EDB7BC295374BFC70DCA738C0C4AED7CBC4EFF7D5DED08AD8E0BEE35B6F73E7592D652ADBF5310218B790501F6657B51