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DESCRIBE <http://purl.uniprot.org/SHA-384/A310ACEF9FC95410DF3C03CDD9800CCFDD59937E43A4944DF9D120D73141E55AEA0C155F00F70074393E717A02A6183B>
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http://purl.uniprot.org/SHA-384/A310ACEF9FC95410DF3C03CDD9800CCFDD59937E43A4944DF9D120D73141E55AEA0C155F00F70074393E717A02A6183B
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A310ACEF9FC95410DF3C03CDD9800CCFDD59937E43A4944DF9D120D73141E55AEA0C155F00F70074393E717A02A6183B
http://www.w3.org/2000/01/rdf-schema#comment
"Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_F13C2EEB58D336030474ADA75DCB96B8C63D141206CE844699E47B470CEE50C1892300D34772B3D7FB9B6246D36D1C49
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A310ACEF9FC95410DF3C03CDD9800CCFDD59937E43A4944DF9D120D73141E55AEA0C155F00F70074393E717A02A6183B
http://purl.uniprot.org/uniprot/E9Q986
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A310ACEF9FC95410DF3C03CDD9800CCFDD59937E43A4944DF9D120D73141E55AEA0C155F00F70074393E717A02A6183B
http://purl.uniprot.org/uniprot/#_E9Q986-mappedCitation-32196547
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A310ACEF9FC95410DF3C03CDD9800CCFDD59937E43A4944DF9D120D73141E55AEA0C155F00F70074393E717A02A6183B