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DESCRIBE <http://purl.uniprot.org/SHA-384/879FB1A2687DDC8023942994B7CD1207C03870FA4118F04BAA441E5A987078F87C8971EC03C76808721364C497F00F5B>
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http://purl.uniprot.org/SHA-384/879FB1A2687DDC8023942994B7CD1207C03870FA4118F04BAA441E5A987078F87C8971EC03C76808721364C497F00F5B
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/879FB1A2687DDC8023942994B7CD1207C03870FA4118F04BAA441E5A987078F87C8971EC03C76808721364C497F00F5B
http://www.w3.org/2000/01/rdf-schema#comment
"EXT1 mutations are associated with a more severe hereditary multiple exostoses phenotype than other EXT forms."
xsd:string
http://purl.uniprot.org/uniprot/#_61EB6F30CC585137D7A8C1F0AD952C33DF5D21234ED6B825453A125F5DC2CEDA8DCB0E3BBEA37A2CB3D34DDB8EA0AA89
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/879FB1A2687DDC8023942994B7CD1207C03870FA4118F04BAA441E5A987078F87C8971EC03C76808721364C497F00F5B
http://purl.uniprot.org/uniprot/D7RTA7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/879FB1A2687DDC8023942994B7CD1207C03870FA4118F04BAA441E5A987078F87C8971EC03C76808721364C497F00F5B
http://purl.uniprot.org/uniprot/#_D7RTA7-mappedCitation-17676624
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/879FB1A2687DDC8023942994B7CD1207C03870FA4118F04BAA441E5A987078F87C8971EC03C76808721364C497F00F5B