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DESCRIBE <http://purl.uniprot.org/SHA-384/4ADE557FCF67BA523D32A7A5A9ECCCA216FF58E7944786776348580ADD476F0B2C6771F77CF382FD1DDF10884569385D>
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http://purl.uniprot.org/SHA-384/4ADE557FCF67BA523D32A7A5A9ECCCA216FF58E7944786776348580ADD476F0B2C6771F77CF382FD1DDF10884569385D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4ADE557FCF67BA523D32A7A5A9ECCCA216FF58E7944786776348580ADD476F0B2C6771F77CF382FD1DDF10884569385D
http://www.w3.org/2000/01/rdf-schema#comment
"The c.301_302delAG homozygous genotype had a high frequency of 38% reaching 100% in group with familial cases of multiple pituitary hormone deficiency and 16% in group with sporadic forms of MPHD."
xsd:string
http://purl.uniprot.org/uniprot/#_79436F3075FD6E8C00739BD2F7FCD4ADDAB90EFD76202C237D52846D7734C6DA7701D8BEC9561F648F4EC1A38EFD1677
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4ADE557FCF67BA523D32A7A5A9ECCCA216FF58E7944786776348580ADD476F0B2C6771F77CF382FD1DDF10884569385D
http://purl.uniprot.org/uniprot/O75360
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4ADE557FCF67BA523D32A7A5A9ECCCA216FF58E7944786776348580ADD476F0B2C6771F77CF382FD1DDF10884569385D
http://purl.uniprot.org/uniprot/#_O75360-mappedCitation-25581745
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4ADE557FCF67BA523D32A7A5A9ECCCA216FF58E7944786776348580ADD476F0B2C6771F77CF382FD1DDF10884569385D