Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_provenance.
- NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_assertion description "[Our case confirms that the inv(11) is a rare chromosomal translocation that is associated with therapy-related or de novo myeloid malignancy and involves NUP98 and DDX10 but not MLL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_provenance.
- NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_assertion evidence source_evidence_literature NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_provenance.
- NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_assertion SIO_000772 10222653 NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_provenance.
- NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_assertion wasDerivedFrom befree-20140225 NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_provenance.
- NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_assertion wasGeneratedBy ECO_0000203 NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP839198.RAGWxlnfCBx685Mqdx4SIF5W1An1lgHEH3DDI_gZ7PkOA130_provenance.