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DESCRIBE <http://purl.uniprot.org/SHA-384/66A80A62E54C30B6338E4F8BAD5A150948EEECD1CF89EE4C23741AD78E4A0589F9F9ACB8B7534F364BBA5E60F68A9FA0>
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http://purl.uniprot.org/SHA-384/66A80A62E54C30B6338E4F8BAD5A150948EEECD1CF89EE4C23741AD78E4A0589F9F9ACB8B7534F364BBA5E60F68A9FA0
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/66A80A62E54C30B6338E4F8BAD5A150948EEECD1CF89EE4C23741AD78E4A0589F9F9ACB8B7534F364BBA5E60F68A9FA0
http://www.w3.org/2000/01/rdf-schema#comment
"Germline PTCH1 mutations are linked to nevoid basal cell carcinoma syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_36728D9AB72917F8534FB139D191A5FDB74998CA0C8272F44D624F68242F9D580B7F6624DC7140AB36D26C7D19E3AF4A
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/66A80A62E54C30B6338E4F8BAD5A150948EEECD1CF89EE4C23741AD78E4A0589F9F9ACB8B7534F364BBA5E60F68A9FA0
http://purl.uniprot.org/uniprot/Q13635
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/66A80A62E54C30B6338E4F8BAD5A150948EEECD1CF89EE4C23741AD78E4A0589F9F9ACB8B7534F364BBA5E60F68A9FA0
http://purl.uniprot.org/uniprot/#_Q13635-mappedCitation-24517962
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/66A80A62E54C30B6338E4F8BAD5A150948EEECD1CF89EE4C23741AD78E4A0589F9F9ACB8B7534F364BBA5E60F68A9FA0