Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_provenance.
- NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_assertion description "[The DDX11-deficient patient represents another cohesinopathy, besides Cornelia de Lange syndrome and Roberts syndrome, and shows that DDX11 functions at the interface between DNA repair and sister chromatid cohesion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_provenance.
- NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_assertion evidence source_evidence_literature NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_provenance.
- NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_assertion SIO_000772 20137776 NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_provenance.
- NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_assertion wasDerivedFrom befree-20150227 NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_provenance.
- NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_assertion wasGeneratedBy ECO_0000203 NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP351781.RAry4VA2LjuZ4AjvGOhI36RQHskOSs38QKSUX4aaThOW8130_provenance.