Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_provenance.
- befree-2016 importedOn "2016-02-19" NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_provenance.
- NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_assertion wasGeneratedBy ECO_0000203 NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_provenance.
- NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_assertion wasDerivedFrom befree-2016 NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_provenance.
- NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_assertion SIO_000772 21098271 NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_provenance.
- NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_assertion evidence source_evidence_literature NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_provenance.
- NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_assertion description "[Finally, two cases had partial deletions of AT rich interactive domain 5B (ARID5B), indicating that acquired as well as constitutional variants in this locus may be associated with pediatric ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853904.RApNAwCg5Uxg9M-YP1YvwOIwL9zse32qqc4TqWCgY6gLo130_provenance.