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DESCRIBE <http://purl.uniprot.org/SHA-384/61FC3A3FEB152192FF29D6313ED53758146D90BAAC24330D6094B63AE66513AC1C3DBAB4E760D03261E3933739F0F5E2>
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http://purl.uniprot.org/SHA-384/61FC3A3FEB152192FF29D6313ED53758146D90BAAC24330D6094B63AE66513AC1C3DBAB4E760D03261E3933739F0F5E2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/61FC3A3FEB152192FF29D6313ED53758146D90BAAC24330D6094B63AE66513AC1C3DBAB4E760D03261E3933739F0F5E2
http://www.w3.org/2000/01/rdf-schema#comment
"Neuroligin mutations most probably represent rare causes of autism; it is unlikely that the allelic variants in any of these genes would be major risk factors for autism."
xsd:string
http://purl.uniprot.org/uniprot/#_6DE5551B332F0F8ABC08EABD204266EA04662DD6304289D0D29D0522A8E8716377D21EBE7A695007C2990F34A91A7B62
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/61FC3A3FEB152192FF29D6313ED53758146D90BAAC24330D6094B63AE66513AC1C3DBAB4E760D03261E3933739F0F5E2
http://purl.uniprot.org/uniprot/Q6MZK0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/61FC3A3FEB152192FF29D6313ED53758146D90BAAC24330D6094B63AE66513AC1C3DBAB4E760D03261E3933739F0F5E2
http://purl.uniprot.org/uniprot/#_Q6MZK0-mappedCitation-16077734
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/61FC3A3FEB152192FF29D6313ED53758146D90BAAC24330D6094B63AE66513AC1C3DBAB4E760D03261E3933739F0F5E2