Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_provenance.
- NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_assertion description "[The chromosomal abnormality der(17)t(12;17)(q13;p13) is very rare in hematologic malignancies, and has been reported in only two patients with therapy-related acute myeloid leukemia (t-AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_provenance.
- NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_assertion evidence source_evidence_literature NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_provenance.
- NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_assertion SIO_000772 19155067 NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_provenance.
- NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_assertion wasDerivedFrom befree-20150227 NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_provenance.
- NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_assertion wasGeneratedBy ECO_0000203 NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP289520.RAAKhQ7WtATfL9hY5jABA6OSl2aQB8suCviA-bDVZ5XTg130_provenance.