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DESCRIBE <http://purl.uniprot.org/SHA-384/4CD5C1CF315869E11F5136036484F73EF46ABDED73B4C8D11AA41B7BEE666E791C2B040310E923BDFE49C093D3A5BAEA>
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http://purl.uniprot.org/SHA-384/4CD5C1CF315869E11F5136036484F73EF46ABDED73B4C8D11AA41B7BEE666E791C2B040310E923BDFE49C093D3A5BAEA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4CD5C1CF315869E11F5136036484F73EF46ABDED73B4C8D11AA41B7BEE666E791C2B040310E923BDFE49C093D3A5BAEA
http://www.w3.org/2000/01/rdf-schema#comment
"Identification of two CUL7 variants in two Chinese families with 3-M syndrome by whole-exome sequencing."
xsd:string
http://purl.uniprot.org/uniprot/#_50C7634544769C34522A691F97D3B66CC56FEF43C053B3CB273F5110D22E576AD81F1BBADCA2C6062295F7E8A5A07B48
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4CD5C1CF315869E11F5136036484F73EF46ABDED73B4C8D11AA41B7BEE666E791C2B040310E923BDFE49C093D3A5BAEA
http://purl.uniprot.org/uniprot/L8E835
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4CD5C1CF315869E11F5136036484F73EF46ABDED73B4C8D11AA41B7BEE666E791C2B040310E923BDFE49C093D3A5BAEA
http://purl.uniprot.org/uniprot/#_L8E835-mappedCitation-32141654
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4CD5C1CF315869E11F5136036484F73EF46ABDED73B4C8D11AA41B7BEE666E791C2B040310E923BDFE49C093D3A5BAEA