Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_assertion> ?p ?o ?g. }
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- NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_assertion type Assertion NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_head.
- 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.
- NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_assertion evidence source_evidence_literature NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_provenance.
- NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_assertion SIO_000772 19203578 NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_provenance.
- NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_assertion wasDerivedFrom befree-2016 NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_provenance.
- NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_assertion wasGeneratedBy ECO_0000203 NP719414.RALr0Kic8SssddE9JSLLiQu6ewvT9EbxuEkETkZwVYOkM130_provenance.