Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_provenance.
- befree-2016 importedOn "2016-02-19" NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_provenance.
- NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_assertion wasGeneratedBy ECO_0000203 NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_provenance.
- NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_assertion wasDerivedFrom befree-2016 NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_provenance.
- NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_assertion SIO_000772 19203578 NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_provenance.
- NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_assertion evidence source_evidence_literature NP719416.RApa_2zeZL4iTjeRMpN2FPdhc4Bg0JvjpYuNiK88NEi0o130_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.