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DESCRIBE <http://purl.uniprot.org/SHA-384/4881573D8DB3F70BAC525216D9BB81E52676EC1E6189CFC1E5AA6B548E84C3388FFF7ABC7D54DD27E01C8AB94250F9D8>
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http://purl.uniprot.org/SHA-384/4881573D8DB3F70BAC525216D9BB81E52676EC1E6189CFC1E5AA6B548E84C3388FFF7ABC7D54DD27E01C8AB94250F9D8
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4881573D8DB3F70BAC525216D9BB81E52676EC1E6189CFC1E5AA6B548E84C3388FFF7ABC7D54DD27E01C8AB94250F9D8
http://www.w3.org/2000/01/rdf-schema#comment
"DNA mutation analysis revealed mutations in exon 4 of MECP2 gene in two Tunisian patients affected with Rett syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_C41F7E03B0D238AE9B951A121D51FB0546DC708EA73C82D9805CD11C3E79F50C34D68FF64731E78159FFA98FFF6F9C93
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4881573D8DB3F70BAC525216D9BB81E52676EC1E6189CFC1E5AA6B548E84C3388FFF7ABC7D54DD27E01C8AB94250F9D8
http://purl.uniprot.org/uniprot/D3YJ43
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4881573D8DB3F70BAC525216D9BB81E52676EC1E6189CFC1E5AA6B548E84C3388FFF7ABC7D54DD27E01C8AB94250F9D8
http://purl.uniprot.org/uniprot/#_D3YJ43-mappedCitation-19309283
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4881573D8DB3F70BAC525216D9BB81E52676EC1E6189CFC1E5AA6B548E84C3388FFF7ABC7D54DD27E01C8AB94250F9D8