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DESCRIBE <http://purl.uniprot.org/SHA-384/7759F066D7B674CE4248C0A644EAEA98570A54E338B71650E01AEEC7E97D90BBAFB9A4FC5B84B62567F39FA07FA1EA14>
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http://purl.uniprot.org/SHA-384/7759F066D7B674CE4248C0A644EAEA98570A54E338B71650E01AEEC7E97D90BBAFB9A4FC5B84B62567F39FA07FA1EA14
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7759F066D7B674CE4248C0A644EAEA98570A54E338B71650E01AEEC7E97D90BBAFB9A4FC5B84B62567F39FA07FA1EA14
http://www.w3.org/2000/01/rdf-schema#comment
"This review summarizes the broad range of phenotypes resulting from mutations in MECP2 which is responsible for Rett syndrome in 95% of individuals with the disorder."
xsd:string
http://purl.uniprot.org/uniprot/#_A4FF689A9D9D5581D73AA398E9ADA33529457F2BF223D47B32DF5FFC1CA99525C7DC18FC55210A981858E2CAFBBA5F99
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7759F066D7B674CE4248C0A644EAEA98570A54E338B71650E01AEEC7E97D90BBAFB9A4FC5B84B62567F39FA07FA1EA14
http://purl.uniprot.org/uniprot/P51608
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7759F066D7B674CE4248C0A644EAEA98570A54E338B71650E01AEEC7E97D90BBAFB9A4FC5B84B62567F39FA07FA1EA14
http://purl.uniprot.org/uniprot/#_P51608-mappedCitation-21825235
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7759F066D7B674CE4248C0A644EAEA98570A54E338B71650E01AEEC7E97D90BBAFB9A4FC5B84B62567F39FA07FA1EA14