Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_provenance.
- NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_assertion description "[The t(12;21) is a recurring chromosomal abnormality in acute lymphoblastic leukaemias (ALLs) which results in the production of an ETV6-AML1 fusion gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_provenance.
- NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_assertion evidence source_evidence_literature NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_provenance.
- NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_assertion SIO_000772 9233592 NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_provenance.
- NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_assertion wasDerivedFrom befree-2016 NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_provenance.
- NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_assertion wasGeneratedBy ECO_0000203 NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1377295.RA6fQDZOqYapaimHdSqqtHRkuG_RxGPsxurOkn5vjRGn0130_provenance.