Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance.
- NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_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." NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance.
- NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_assertion evidence source_evidence_literature NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance.
- NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_assertion SIO_000772 20137776 NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance.
- NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_assertion wasDerivedFrom befree-20140225 NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance.
- NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_assertion wasGeneratedBy ECO_0000203 NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP809221.RAwfcRkJV_QPG1nn6i438M4nJfKc9ikD2Yv7Ga_Hn58o0130_provenance.