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DESCRIBE <http://purl.uniprot.org/SHA-384/C954CD2DE3D1153128160D8BD360CD60D4EAE3E84261E3D064D0D326D6F9C84476A64B7C47A3F5ABB93AD4A92D1F88A3>
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http://purl.uniprot.org/SHA-384/C954CD2DE3D1153128160D8BD360CD60D4EAE3E84261E3D064D0D326D6F9C84476A64B7C47A3F5ABB93AD4A92D1F88A3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C954CD2DE3D1153128160D8BD360CD60D4EAE3E84261E3D064D0D326D6F9C84476A64B7C47A3F5ABB93AD4A92D1F88A3
http://www.w3.org/2000/01/rdf-schema#comment
"The structural perturbation resulting from mutation of this single amino acid reveals the molecular mechanism underlying PGM1 deficiency in these missense variants."
xsd:string
http://purl.uniprot.org/uniprot/#_E4FBC76A7E1E54CA80BBD5B334DF594B796A6006881C03C59264B521C101D704FE48CFDF323253C2843F5CA77F82A534
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/C954CD2DE3D1153128160D8BD360CD60D4EAE3E84261E3D064D0D326D6F9C84476A64B7C47A3F5ABB93AD4A92D1F88A3
http://purl.uniprot.org/uniprot/B4DDQ8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C954CD2DE3D1153128160D8BD360CD60D4EAE3E84261E3D064D0D326D6F9C84476A64B7C47A3F5ABB93AD4A92D1F88A3
http://purl.uniprot.org/uniprot/#_B4DDQ8-mappedCitation-28117557
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C954CD2DE3D1153128160D8BD360CD60D4EAE3E84261E3D064D0D326D6F9C84476A64B7C47A3F5ABB93AD4A92D1F88A3