Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_provenance.
- 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.
- NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_assertion evidence source_evidence_literature NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_provenance.
- NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_assertion SIO_000772 19203578 NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_provenance.
- NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_assertion wasDerivedFrom befree-20140225 NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_provenance.
- NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_assertion wasGeneratedBy ECO_0000203 NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP730060.RAunbCs3XBmYAZBDi8FjW4H7FNqGySqNPt0YlfaZ-KNs4130_provenance.