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DESCRIBE <http://purl.uniprot.org/SHA-384/EC64C5E885ABEC34D840AF0FCA8546A0D9BF76A28806BE14F2F89873778620D37C6ADEB9FCD72D091CB827DD71B27542>
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http://purl.uniprot.org/SHA-384/EC64C5E885ABEC34D840AF0FCA8546A0D9BF76A28806BE14F2F89873778620D37C6ADEB9FCD72D091CB827DD71B27542
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/EC64C5E885ABEC34D840AF0FCA8546A0D9BF76A28806BE14F2F89873778620D37C6ADEB9FCD72D091CB827DD71B27542
http://www.w3.org/2000/01/rdf-schema#comment
"ATP7A mutations leading to Menkes disease and occipital horn syndrome in human and animal models (review)"
xsd:string
http://purl.uniprot.org/uniprot/#_194EF2411AAFFF0981CAEDCD81262C6C81E1B6A23F7DEDDFE66431F8AB63147082B03AE939D32CE0663FB5754779884E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/EC64C5E885ABEC34D840AF0FCA8546A0D9BF76A28806BE14F2F89873778620D37C6ADEB9FCD72D091CB827DD71B27542
http://purl.uniprot.org/uniprot/Q3T9Y7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EC64C5E885ABEC34D840AF0FCA8546A0D9BF76A28806BE14F2F89873778620D37C6ADEB9FCD72D091CB827DD71B27542
http://purl.uniprot.org/uniprot/#_Q3T9Y7-mappedCitation-23281160
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EC64C5E885ABEC34D840AF0FCA8546A0D9BF76A28806BE14F2F89873778620D37C6ADEB9FCD72D091CB827DD71B27542