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DESCRIBE <http://purl.uniprot.org/SHA-384/D417877C179EA327D8AB0A2C25EDAF64BE5C846492734205247327D0BCAB6A811CB06D5A0AAC690BEB6563069E24BFA5>
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http://purl.uniprot.org/SHA-384/D417877C179EA327D8AB0A2C25EDAF64BE5C846492734205247327D0BCAB6A811CB06D5A0AAC690BEB6563069E24BFA5
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/D417877C179EA327D8AB0A2C25EDAF64BE5C846492734205247327D0BCAB6A811CB06D5A0AAC690BEB6563069E24BFA5
http://www.w3.org/2000/01/rdf-schema#comment
"Absence of DNMT1o results in the partial loss of methylation at imprinted differentially methylated domain sequences in the embryo and the placenta with structural abnormalities of all tissue layers."
xsd:string
http://purl.uniprot.org/uniprot/#_7BB1A185A76FFD73DE3874D21039E97A6270C3393329A1D73F09B1D08EBDCC92E6F05E38004687D898DEEC3D9EA5219E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/D417877C179EA327D8AB0A2C25EDAF64BE5C846492734205247327D0BCAB6A811CB06D5A0AAC690BEB6563069E24BFA5
http://purl.uniprot.org/uniprot/Q3UHZ3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D417877C179EA327D8AB0A2C25EDAF64BE5C846492734205247327D0BCAB6A811CB06D5A0AAC690BEB6563069E24BFA5
http://purl.uniprot.org/uniprot/#_Q3UHZ3-mappedCitation-23085235
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D417877C179EA327D8AB0A2C25EDAF64BE5C846492734205247327D0BCAB6A811CB06D5A0AAC690BEB6563069E24BFA5