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DESCRIBE <http://purl.uniprot.org/SHA-384/FBED5F5D3BC9BAEC948EAB1AA47878EE43A7E577C2D087D55F8338DE4F5EC0685933615DAC2991A95FBC77EB9CB69FA5>
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http://purl.uniprot.org/SHA-384/FBED5F5D3BC9BAEC948EAB1AA47878EE43A7E577C2D087D55F8338DE4F5EC0685933615DAC2991A95FBC77EB9CB69FA5
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/FBED5F5D3BC9BAEC948EAB1AA47878EE43A7E577C2D087D55F8338DE4F5EC0685933615DAC2991A95FBC77EB9CB69FA5
http://www.w3.org/2000/01/rdf-schema#comment
"Results suggest that there is no specific mutation responsible for the Tetralogy of Fallot phenotype in the Vangl2 gene [Vangl2]"
xsd:string
http://purl.uniprot.org/uniprot/#_819C8FCEEE826A0DDF71C262A6FB408A8E6B8D2E3602F663541885A9A171828C4C9798D4046D5F659A7602A9D39C5C45
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/FBED5F5D3BC9BAEC948EAB1AA47878EE43A7E577C2D087D55F8338DE4F5EC0685933615DAC2991A95FBC77EB9CB69FA5
http://purl.uniprot.org/uniprot/A8K4L6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FBED5F5D3BC9BAEC948EAB1AA47878EE43A7E577C2D087D55F8338DE4F5EC0685933615DAC2991A95FBC77EB9CB69FA5
http://purl.uniprot.org/uniprot/#_A8K4L6-mappedCitation-18034999
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FBED5F5D3BC9BAEC948EAB1AA47878EE43A7E577C2D087D55F8338DE4F5EC0685933615DAC2991A95FBC77EB9CB69FA5