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DESCRIBE <http://purl.uniprot.org/SHA-384/9C4BB4174D6BEB2B8FF933D8CC4514EFC31BA54E2A4A7673B9E567084A20468F0697D2D81429C5602EA335A61919646A>
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http://purl.uniprot.org/SHA-384/9C4BB4174D6BEB2B8FF933D8CC4514EFC31BA54E2A4A7673B9E567084A20468F0697D2D81429C5602EA335A61919646A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9C4BB4174D6BEB2B8FF933D8CC4514EFC31BA54E2A4A7673B9E567084A20468F0697D2D81429C5602EA335A61919646A
http://www.w3.org/2000/01/rdf-schema#comment
"Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of 18q12.3 encompassing SETBP1."
xsd:string
http://purl.uniprot.org/uniprot/#_0981BE32DE25715713A9ABD4A739C9CC09F4E6218998CB3892FE1D494BDAD4861E29CF697B933083911F53C44324A8B3
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9C4BB4174D6BEB2B8FF933D8CC4514EFC31BA54E2A4A7673B9E567084A20468F0697D2D81429C5602EA335A61919646A
http://purl.uniprot.org/uniprot/Q9Y6X0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9C4BB4174D6BEB2B8FF933D8CC4514EFC31BA54E2A4A7673B9E567084A20468F0697D2D81429C5602EA335A61919646A
http://purl.uniprot.org/uniprot/#_Q9Y6X0-mappedCitation-36113068
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9C4BB4174D6BEB2B8FF933D8CC4514EFC31BA54E2A4A7673B9E567084A20468F0697D2D81429C5602EA335A61919646A