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DESCRIBE <http://purl.uniprot.org/SHA-384/4F49D461762EF6C0124414BD1C37972C13C1217C1E51A472B4E0BD91CA8FD4A1309AC9482FC6A2D3D34F88BCF3E7B7CC>
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http://purl.uniprot.org/SHA-384/4F49D461762EF6C0124414BD1C37972C13C1217C1E51A472B4E0BD91CA8FD4A1309AC9482FC6A2D3D34F88BCF3E7B7CC
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4F49D461762EF6C0124414BD1C37972C13C1217C1E51A472B4E0BD91CA8FD4A1309AC9482FC6A2D3D34F88BCF3E7B7CC
http://www.w3.org/2000/01/rdf-schema#comment
"SETBP1 and SRSF2 are the most common somatic genetic abnormalities in patients with myeloid neoplasms carrying isochrmosome 17(q10) and may be important drivers of disease pathogenesis."
xsd:string
http://purl.uniprot.org/uniprot/#_2FAB5677BD5F6093BC64DCE34AA2EC1A317E815DACA739B01AFD0063CA44A84C079F76C4DD7EBE8BBEBE9BA8C85BDDA1
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4F49D461762EF6C0124414BD1C37972C13C1217C1E51A472B4E0BD91CA8FD4A1309AC9482FC6A2D3D34F88BCF3E7B7CC
http://purl.uniprot.org/uniprot/B3KUY1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4F49D461762EF6C0124414BD1C37972C13C1217C1E51A472B4E0BD91CA8FD4A1309AC9482FC6A2D3D34F88BCF3E7B7CC
http://purl.uniprot.org/uniprot/#_B3KUY1-mappedCitation-24796269
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4F49D461762EF6C0124414BD1C37972C13C1217C1E51A472B4E0BD91CA8FD4A1309AC9482FC6A2D3D34F88BCF3E7B7CC