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DESCRIBE <http://purl.uniprot.org/SHA-384/33F85B32D82E5E82B475EED62B2FC38F901CE80866AD0783BDF26E2F3D2DE466C614B0249D9B14C804860EC295A5FBC5>
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http://purl.uniprot.org/SHA-384/33F85B32D82E5E82B475EED62B2FC38F901CE80866AD0783BDF26E2F3D2DE466C614B0249D9B14C804860EC295A5FBC5
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/33F85B32D82E5E82B475EED62B2FC38F901CE80866AD0783BDF26E2F3D2DE466C614B0249D9B14C804860EC295A5FBC5
http://www.w3.org/2000/01/rdf-schema#comment
"study supports a pathogenic role for heterozygous exonic deletions of NRXN1 in neurodevelopmental disorders"
xsd:string
http://purl.uniprot.org/uniprot/#_548E26A5FC29831224185E78AA0596CE81953EF20065B5CC111E66B800F5F3A788BDAAD14186E9A85B357466A017991B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/33F85B32D82E5E82B475EED62B2FC38F901CE80866AD0783BDF26E2F3D2DE466C614B0249D9B14C804860EC295A5FBC5
http://purl.uniprot.org/uniprot/A0A0D9SEQ7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/33F85B32D82E5E82B475EED62B2FC38F901CE80866AD0783BDF26E2F3D2DE466C614B0249D9B14C804860EC295A5FBC5
http://purl.uniprot.org/uniprot/#_A0A0D9SEQ7-mappedCitation-23533028
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/33F85B32D82E5E82B475EED62B2FC38F901CE80866AD0783BDF26E2F3D2DE466C614B0249D9B14C804860EC295A5FBC5