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DESCRIBE <http://purl.uniprot.org/SHA-384/5B18156BA174E66217C380BB4816CE6EF4A70BD6F4F71B0F45D9D3ECF426522E65EB57A01D0FEA649605F5921F0C0BC2>
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http://purl.uniprot.org/SHA-384/5B18156BA174E66217C380BB4816CE6EF4A70BD6F4F71B0F45D9D3ECF426522E65EB57A01D0FEA649605F5921F0C0BC2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5B18156BA174E66217C380BB4816CE6EF4A70BD6F4F71B0F45D9D3ECF426522E65EB57A01D0FEA649605F5921F0C0BC2
http://www.w3.org/2000/01/rdf-schema#comment
"Nine newly identified individuals refine the phenotype associated with MYT1L mutations."
xsd:string
http://purl.uniprot.org/uniprot/#_6096A7B328D576B4990EF254C95D1E9F6378A10F8E46D14530760A28F4154FB9CCD55D15998E7826A6815922299861EE
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5B18156BA174E66217C380BB4816CE6EF4A70BD6F4F71B0F45D9D3ECF426522E65EB57A01D0FEA649605F5921F0C0BC2
http://purl.uniprot.org/uniprot/Q9UL68
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5B18156BA174E66217C380BB4816CE6EF4A70BD6F4F71B0F45D9D3ECF426522E65EB57A01D0FEA649605F5921F0C0BC2
http://purl.uniprot.org/uniprot/#_Q9UL68-mappedCitation-32065501
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5B18156BA174E66217C380BB4816CE6EF4A70BD6F4F71B0F45D9D3ECF426522E65EB57A01D0FEA649605F5921F0C0BC2