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DESCRIBE <http://purl.uniprot.org/SHA-384/7A7AE48A44F942D112735C4246789E540F0C25E6C30D30A6F3DA05525C084B3EE3B8838F517472E0A37891F26FF594A1>
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http://purl.uniprot.org/SHA-384/7A7AE48A44F942D112735C4246789E540F0C25E6C30D30A6F3DA05525C084B3EE3B8838F517472E0A37891F26FF594A1
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7A7AE48A44F942D112735C4246789E540F0C25E6C30D30A6F3DA05525C084B3EE3B8838F517472E0A37891F26FF594A1
http://www.w3.org/2000/01/rdf-schema#comment
"Data suggest that the microcephaly observed in patients with MCPH1 deficiencies is due to disruption of the ATR-BRCA1-Chk1 signaling pathway that is also disrupted in Seckel syndrome patients."
xsd:string
http://purl.uniprot.org/uniprot/#_E21F287EAA757229A8F852E5D837AD9242BD92C7F06E515281E1F62952BCF56F033D6DE85E541242208C8B0CB96A5B63
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7A7AE48A44F942D112735C4246789E540F0C25E6C30D30A6F3DA05525C084B3EE3B8838F517472E0A37891F26FF594A1
http://purl.uniprot.org/uniprot/Q6RA50
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7A7AE48A44F942D112735C4246789E540F0C25E6C30D30A6F3DA05525C084B3EE3B8838F517472E0A37891F26FF594A1
http://purl.uniprot.org/uniprot/#_Q6RA50-mappedCitation-16217032
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7A7AE48A44F942D112735C4246789E540F0C25E6C30D30A6F3DA05525C084B3EE3B8838F517472E0A37891F26FF594A1