Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_provenance.
- NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_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." NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_provenance.
- NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_assertion evidence source_evidence_literature NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_provenance.
- NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_assertion SIO_000772 16803569 NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_provenance.
- NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_assertion wasDerivedFrom befree-20150227 NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_provenance.
- NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_assertion wasGeneratedBy ECO_0000203 NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_provenance.
- befree-20150227 importedOn "2015-02-27" NP394413.RAawvgbqvToRBMJ_xSUCRDa3slMdRwAVfvWL-A8wsXQog130_provenance.