Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_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." NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_provenance.
- 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.
- 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.
- NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_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." NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_provenance.
- 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 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.
- NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_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." NP271562.RAtRO7vkVocIJzS24dEAqiEz36nOpLcO49dkzLJSA65oo130_provenance.
- NP755217.RAjMcHaU1mNqdoOtba5UZb7UPSgHDML4JTFuV8RjFRZfI130_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." NP755217.RAjMcHaU1mNqdoOtba5UZb7UPSgHDML4JTFuV8RjFRZfI130_provenance.
- NP719415.RAnRXnjweRZxfDDvzX1rWq745m3zwKUaOY4c9-0hqfOvs130_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." NP719415.RAnRXnjweRZxfDDvzX1rWq745m3zwKUaOY4c9-0hqfOvs130_provenance.
- NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_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." NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_provenance.
- NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_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." NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_provenance.