Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance.
- NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance.
- NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_assertion evidence source_evidence_literature NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance.
- NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_assertion SIO_000772 20137776 NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance.
- NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_assertion wasDerivedFrom befree-20150227 NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance.
- NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_assertion wasGeneratedBy ECO_0000203 NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP351793.RAUffPR7MgzlXcI6T6aVoKm5RZgW2SSi2uZ8tOzbgi-TY130_provenance.