Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_provenance.
- NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_assertion description "[No evidence of significant silencing of Fanconi genes FANCF and FANCB or Nijmegen breakage syndrome gene NBS1 by DNA hyper-methylation in sporadic childhood leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_provenance.
- NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_assertion evidence source_evidence_literature NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_provenance.
- NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_assertion SIO_000772 16803569 NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_provenance.
- NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_assertion wasDerivedFrom befree-2016 NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_provenance.
- NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_assertion wasGeneratedBy ECO_0000203 NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_provenance.
- befree-2016 importedOn "2016-02-19" NP556762.RABMJ2t7p3O1gnyAt1fDcKibGTsAbYnHuOZdTw-o2A8zY130_provenance.