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- source_evidence_literature type ECO_0000212 NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_provenance.
- NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_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." NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_provenance.
- NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_assertion evidence source_evidence_literature NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_provenance.
- NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_assertion SIO_000772 16803569 NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_provenance.
- NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_assertion wasDerivedFrom befree-20150227 NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_provenance.
- NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_assertion wasGeneratedBy ECO_0000203 NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584963.RAHyxIYhOicg9kVznBilYf0iGX7XnYRdv63P40BJWhaq8130_provenance.