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DESCRIBE <http://purl.uniprot.org/SHA-384/CBCF0B0E33DA09B72E5FC2E366F96D7127908F1800339A53B8EDD5FAF6EDE2B3FE27E22474C7FF0914A5A28385C87543>
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http://purl.uniprot.org/SHA-384/CBCF0B0E33DA09B72E5FC2E366F96D7127908F1800339A53B8EDD5FAF6EDE2B3FE27E22474C7FF0914A5A28385C87543
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CBCF0B0E33DA09B72E5FC2E366F96D7127908F1800339A53B8EDD5FAF6EDE2B3FE27E22474C7FF0914A5A28385C87543
http://www.w3.org/2000/01/rdf-schema#comment
"knockdown of MCM2 or MCM6 could significantly inhibit foci forming of MDC1 in TE-1 nuclei in response to bleomycin-induced DNA damage (p < 0.001). This study indicates the direct interaction between MDC1 and MCMs in TE-1 nuclei."
xsd:string
http://purl.uniprot.org/uniprot/#_4AE37BB5945F0D363D285052A63F495B14ED052957C073BED929F81703F48A3CDDC1D9282CADFD66FF1E45ED05F86C09
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CBCF0B0E33DA09B72E5FC2E366F96D7127908F1800339A53B8EDD5FAF6EDE2B3FE27E22474C7FF0914A5A28385C87543
http://purl.uniprot.org/uniprot/A0A1U9XBC1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CBCF0B0E33DA09B72E5FC2E366F96D7127908F1800339A53B8EDD5FAF6EDE2B3FE27E22474C7FF0914A5A28385C87543
http://purl.uniprot.org/uniprot/#_A0A1U9XBC1-mappedCitation-27908247
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CBCF0B0E33DA09B72E5FC2E366F96D7127908F1800339A53B8EDD5FAF6EDE2B3FE27E22474C7FF0914A5A28385C87543