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DESCRIBE <http://purl.uniprot.org/SHA-384/D574C5FC9AC0EADA0DEDCB6FE2500076DEB6217DA39469A32741D6DD8D2337BD64B9E8DB694BBEF28D687BD2E41DD706>
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http://purl.uniprot.org/SHA-384/D574C5FC9AC0EADA0DEDCB6FE2500076DEB6217DA39469A32741D6DD8D2337BD64B9E8DB694BBEF28D687BD2E41DD706
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/D574C5FC9AC0EADA0DEDCB6FE2500076DEB6217DA39469A32741D6DD8D2337BD64B9E8DB694BBEF28D687BD2E41DD706
http://www.w3.org/2000/01/rdf-schema#comment
"neurobeachin encoding gene is disrupted in a patient with a de novo translocation t(5;13) (q12.1;q13.2) idiopathic autism and no family history of autism"
xsd:string
http://purl.uniprot.org/uniprot/#_024B983B25529D5BBFCE92A28F8527B98E0BBE3544E061B1AA79A6F450C8E8ED4DBBCCE704B96E120E52CD1149CF5DD7
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/D574C5FC9AC0EADA0DEDCB6FE2500076DEB6217DA39469A32741D6DD8D2337BD64B9E8DB694BBEF28D687BD2E41DD706
http://purl.uniprot.org/uniprot/B3KXQ8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D574C5FC9AC0EADA0DEDCB6FE2500076DEB6217DA39469A32741D6DD8D2337BD64B9E8DB694BBEF28D687BD2E41DD706
http://purl.uniprot.org/uniprot/#_B3KXQ8-mappedCitation-12746398
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D574C5FC9AC0EADA0DEDCB6FE2500076DEB6217DA39469A32741D6DD8D2337BD64B9E8DB694BBEF28D687BD2E41DD706