Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_assertion> ?p ?o ?g. }
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- NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_assertion type Assertion NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_head.
- NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_assertion description "[These RNF168-dependent chromatin modifications orchestrate the accumulation of 53BP1 and BRCA1 to DNA lesions, and their loss is the likely cause of the cellular and developmental phenotypes associated with RIDDLE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_provenance.
- NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_assertion evidence source_evidence_literature NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_provenance.
- NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_assertion SIO_000772 19203578 NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_provenance.
- NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_assertion wasDerivedFrom befree-20150227 NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_provenance.
- NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_assertion wasGeneratedBy ECO_0000203 NP977631.RATzPtaT1fFZ4wN6WcCMdTl7GbwqbeSH0blYhRsYwrZdc130_provenance.