Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_provenance.
- NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_assertion description "[High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_provenance.
- NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_assertion evidence source_evidence_literature NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_provenance.
- NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_assertion SIO_000772 16646086 NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_provenance.
- NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_assertion wasDerivedFrom befree-20150227 NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_provenance.
- NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_assertion wasGeneratedBy ECO_0000203 NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP452470.RAISrWfD29lQUgmCH94sNJTXl1oEImY7OtRw_Ies1bw4I130_provenance.