Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_assertion> ?p ?o ?g. }
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- NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_assertion type Assertion NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_head.
- 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.
- NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_assertion evidence source_evidence_literature NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_provenance.
- NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_assertion SIO_000772 19203578 NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_provenance.
- NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_assertion wasDerivedFrom befree-20140225 NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_provenance.
- NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_assertion wasGeneratedBy ECO_0000203 NP615437.RAOtmGN5qYB8Zs7HO_HkMhY6Ryw4wTvC-4XpEKkPMNxaY130_provenance.