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DESCRIBE <http://purl.uniprot.org/citations/10991689>
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http://purl.uniprot.org/uniprot/P51608#attribution-128F6A12546692421DA028FE8D254464
http://purl.uniprot.org/core/source
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/uniprot/#_P51608-citation-10991689
http://www.w3.org/1999/02/22-rdf-syntax-ns#object
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/citations/10991689
http://www.w3.org/2004/02/skos/core#exactMatch
http://purl.uniprot.org/pubmed/10991689
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/core/author
"Webb T."
xsd:string
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/core/date
"2000"
xsd:gYear
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/core/author
"Hampson K."
xsd:string
http://purl.uniprot.org/citations/10991689
http://xmlns.com/foaf/0.1/primaryTopicOf
https://pubmed.ncbi.nlm.nih.gov/10991689
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/core/title
"Mutations in the MECP2 gene in a cohort of girls with Rett syndrome."
xsd:string
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/core/volume
"37"
xsd:string
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/core/pages
"610-612"
xsd:string
http://purl.uniprot.org/citations/10991689
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/core/author
"Woods C.G."
xsd:string
http://purl.uniprot.org/citations/10991689
http://purl.org/dc/terms/identifier
"doi:10.1136/jmg.37.8.610"
xsd:string
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/core/author
"Latif F."
xsd:string
http://purl.uniprot.org/uniprot/P51608
http://purl.uniprot.org/core/citation
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/citations/10991689
http://purl.uniprot.org/core/name
"J. Med. Genet."
xsd:string