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DESCRIBE <http://purl.uniprot.org/SHA-384/FBC9342E1602810A52B240F78F12EAC399B25065B3C9C7F6D74B15C31676A8AC16959B8D7C973D4E91094A9C50CDBA84>
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http://purl.uniprot.org/SHA-384/FBC9342E1602810A52B240F78F12EAC399B25065B3C9C7F6D74B15C31676A8AC16959B8D7C973D4E91094A9C50CDBA84
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/FBC9342E1602810A52B240F78F12EAC399B25065B3C9C7F6D74B15C31676A8AC16959B8D7C973D4E91094A9C50CDBA84
http://www.w3.org/2000/01/rdf-schema#comment
"The CRELD1 gene is likely to have a major role in causation of AVSD phenotype in selected DS patients."
xsd:string
http://purl.uniprot.org/uniprot/#_7F1D6FF3CD100BC6E5C4C4177F15A82C731511B1A7AA2B3CE215ED402D82240A2702D3D7FF6C91F3133A78352B44B7ED
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/FBC9342E1602810A52B240F78F12EAC399B25065B3C9C7F6D74B15C31676A8AC16959B8D7C973D4E91094A9C50CDBA84
http://purl.uniprot.org/uniprot/Q96HD1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FBC9342E1602810A52B240F78F12EAC399B25065B3C9C7F6D74B15C31676A8AC16959B8D7C973D4E91094A9C50CDBA84
http://purl.uniprot.org/uniprot/#_Q96HD1-mappedCitation-29054759
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FBC9342E1602810A52B240F78F12EAC399B25065B3C9C7F6D74B15C31676A8AC16959B8D7C973D4E91094A9C50CDBA84