Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_provenance.
- NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_assertion description "[We compared clinicopathologic factors, including age, sex, WBC count, cerebrospinal fluid (CSF) involvement, immunophenotype, and blast proliferation rate between B-ALL with RUNX1 amplification (10 cases) and B-ALL with ETV6-RUNX1 translocation (67 cases) in childhood B-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_provenance.
- NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_assertion evidence source_evidence_literature NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_provenance.
- NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_assertion SIO_000772 26185316 NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_provenance.
- NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_assertion wasDerivedFrom befree-2016 NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_provenance.
- NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_assertion wasGeneratedBy ECO_0000203 NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_provenance.
- befree-2016 importedOn "2016-02-19" NP1290339.RAkvrx9cQeaEx3zOFXcIolCj7FUY7S5RH0q4FXbgA-y30130_provenance.