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DESCRIBE <http://purl.uniprot.org/SHA-384/2CF392DBAC4A5922127CE95E10CA02639D306DC18A5FB9E4B6321F6E1A711CAB87F412BF4D7E0CB4E9482D5EC03FF6E8>
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http://purl.uniprot.org/SHA-384/2CF392DBAC4A5922127CE95E10CA02639D306DC18A5FB9E4B6321F6E1A711CAB87F412BF4D7E0CB4E9482D5EC03FF6E8
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/2CF392DBAC4A5922127CE95E10CA02639D306DC18A5FB9E4B6321F6E1A711CAB87F412BF4D7E0CB4E9482D5EC03FF6E8
http://www.w3.org/2000/01/rdf-schema#comment
"A daughter who carried the der Y had the clinical features of Prader-Willi syndrome while a son who carries the der 15 has mild developmental delay and hypogonadism."
xsd:string
http://purl.uniprot.org/uniprot/#_1619481E404BAC0EAB0F7042E1E9E0E1FC2DEA49DC7D478AD2E55C183DD6563DC405AB356F259B8107ABEDE0C225F104
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/2CF392DBAC4A5922127CE95E10CA02639D306DC18A5FB9E4B6321F6E1A711CAB87F412BF4D7E0CB4E9482D5EC03FF6E8
http://purl.uniprot.org/uniprot/Q99928
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2CF392DBAC4A5922127CE95E10CA02639D306DC18A5FB9E4B6321F6E1A711CAB87F412BF4D7E0CB4E9482D5EC03FF6E8
http://purl.uniprot.org/uniprot/#_Q99928-mappedCitation-14981720
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2CF392DBAC4A5922127CE95E10CA02639D306DC18A5FB9E4B6321F6E1A711CAB87F412BF4D7E0CB4E9482D5EC03FF6E8