Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_provenance.
- NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_assertion description "[The recurring chromosomal 9;11 translocation [t(9;11) (p22;q23)] typically is associated with acute monoblastic leukemia, but a number of patients with acute lymphoblastic leukemia also have been reported to have the t(9;11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_provenance.
- NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_assertion evidence source_evidence_literature NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_provenance.
- NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_assertion SIO_000772 1906342 NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_provenance.
- NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_assertion wasDerivedFrom befree-20140225 NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_provenance.
- NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_assertion wasGeneratedBy ECO_0000203 NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP681048.RAsh3aiZ5PnAk3e3g-EQvDW5kxXlvdOOkehtDbLmrz9u0130_provenance.