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- source_evidence_literature type ECO_0000212 NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_provenance.
- NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_assertion description "[We conclude that ras mutations are observed in childhood monosomy 7, though less frequently than in adult MDS, and may play a limited role in the progression of this disease to acute leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_provenance.
- NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_assertion evidence source_evidence_literature NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_provenance.
- NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_assertion SIO_000772 1991170 NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_provenance.
- NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_assertion wasDerivedFrom befree-2016 NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_provenance.
- NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_assertion wasGeneratedBy ECO_0000203 NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_provenance.
- befree-2016 importedOn "2016-02-19" NP775616.RA3psCM18vonKF-Nog3ZgL1WZS4do9ulLbHXa_nMO7Slk130_provenance.