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DESCRIBE <http://purl.uniprot.org/SHA-384/470ECB6240A82CB26CF3FD830B954F8DE091E16C5A1F24DB2964B220ECBB1DC5C602F9B9AE7248BB805281D1458111E5>
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http://purl.uniprot.org/SHA-384/470ECB6240A82CB26CF3FD830B954F8DE091E16C5A1F24DB2964B220ECBB1DC5C602F9B9AE7248BB805281D1458111E5
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/470ECB6240A82CB26CF3FD830B954F8DE091E16C5A1F24DB2964B220ECBB1DC5C602F9B9AE7248BB805281D1458111E5
http://www.w3.org/2000/01/rdf-schema#comment
"NKX2-5 is thus responsible for dominant familial ASD even in consanguineous populations and a wide genetic and phenotypic diversity is characteristic of NKX2-5 mutations in the Lebanese population."
xsd:string
http://purl.uniprot.org/uniprot/#_6B5D5117E1736C3AF399942F0A3CC7330911BEEB61D44A0BF90F7D1F0304D9849BA79AC9D37EDAD4B11A9B5C69AA31FE
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/470ECB6240A82CB26CF3FD830B954F8DE091E16C5A1F24DB2964B220ECBB1DC5C602F9B9AE7248BB805281D1458111E5
http://purl.uniprot.org/uniprot/A0A2R4LFT4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/470ECB6240A82CB26CF3FD830B954F8DE091E16C5A1F24DB2964B220ECBB1DC5C602F9B9AE7248BB805281D1458111E5
http://purl.uniprot.org/uniprot/#_A0A2R4LFT4-mappedCitation-25742962
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/470ECB6240A82CB26CF3FD830B954F8DE091E16C5A1F24DB2964B220ECBB1DC5C602F9B9AE7248BB805281D1458111E5