Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_provenance.
- NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_assertion description "[A recurrent chromosomal abnormality in acute myeloid leukemia is the reciprocal translocation t(8;21) that fuses RUNX1 and ETO genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_provenance.
- NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_assertion evidence source_evidence_literature NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_provenance.
- NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_assertion SIO_000772 26333776 NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_provenance.
- NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_assertion wasDerivedFrom befree-2016 NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_provenance.
- NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_assertion wasGeneratedBy ECO_0000203 NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293588.RASLIHqdb-AIqmXVMKfzY5gV5U-cOwENrUwjKEn64H5UI130_provenance.