Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP123860.RAUVw6nQzQv2mAuyr5I9I6IuIlOEArD2p0y_GhWeVs_Mg#assertion> ?p ?o ?g. }
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- 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." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 19203578 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.