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DESCRIBE <http://purl.uniprot.org/SHA-384/E41F1A4DB55FF413CA58F490F5AFDFEE81B1E57D9AB7BFD55E3558C378706955EF7B4B94A6CEEF5A3858B93821772B80>
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http://purl.uniprot.org/SHA-384/E41F1A4DB55FF413CA58F490F5AFDFEE81B1E57D9AB7BFD55E3558C378706955EF7B4B94A6CEEF5A3858B93821772B80
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E41F1A4DB55FF413CA58F490F5AFDFEE81B1E57D9AB7BFD55E3558C378706955EF7B4B94A6CEEF5A3858B93821772B80
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/#_3382D10058D7F4B4F195A08F2F24849F5B8905D3271C6E13FEDFAAA02E8EDF2228124B01BB32D5E9DFA62214880231E9
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E41F1A4DB55FF413CA58F490F5AFDFEE81B1E57D9AB7BFD55E3558C378706955EF7B4B94A6CEEF5A3858B93821772B80
http://purl.uniprot.org/uniprot/A0A3B3ISW5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E41F1A4DB55FF413CA58F490F5AFDFEE81B1E57D9AB7BFD55E3558C378706955EF7B4B94A6CEEF5A3858B93821772B80
http://purl.uniprot.org/uniprot/#_A0A3B3ISW5-mappedCitation-28859103
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E41F1A4DB55FF413CA58F490F5AFDFEE81B1E57D9AB7BFD55E3558C378706955EF7B4B94A6CEEF5A3858B93821772B80