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DESCRIBE <http://purl.uniprot.org/SHA-384/5B6AA4FBA1B7611684E67857EC6EA3987680876E835DE48F716F420DFBB277D747893A598E6D7C8BBF9CC659FCA94C1B>
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http://purl.uniprot.org/SHA-384/5B6AA4FBA1B7611684E67857EC6EA3987680876E835DE48F716F420DFBB277D747893A598E6D7C8BBF9CC659FCA94C1B
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5B6AA4FBA1B7611684E67857EC6EA3987680876E835DE48F716F420DFBB277D747893A598E6D7C8BBF9CC659FCA94C1B
http://www.w3.org/2000/01/rdf-schema#comment
"This study demonstrates that MYT1L variants are associated with syndromic obesity in humans. The mechanism is related to dysregulated expression of neurodevelopmental genes and altered development of the neuroendocrine hypothalamus"
xsd:string
http://purl.uniprot.org/uniprot/#_D10E629FDBDA0471BCF09D22A61276AB885B6ABC38BA09355B1698F4F0E456D3F4F570FDDEB3D30C335E6DE2249EB4F2
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5B6AA4FBA1B7611684E67857EC6EA3987680876E835DE48F716F420DFBB277D747893A598E6D7C8BBF9CC659FCA94C1B
http://purl.uniprot.org/uniprot/Q9UL68
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5B6AA4FBA1B7611684E67857EC6EA3987680876E835DE48F716F420DFBB277D747893A598E6D7C8BBF9CC659FCA94C1B
http://purl.uniprot.org/uniprot/#_Q9UL68-mappedCitation-28859103
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5B6AA4FBA1B7611684E67857EC6EA3987680876E835DE48F716F420DFBB277D747893A598E6D7C8BBF9CC659FCA94C1B