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- source_evidence_literature type ECO_0000212 NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_provenance.
- NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_assertion description "[Acquired molecular abnormalities (mutations or chromosomal translocations) of the RUNX1 transcription factor gene are frequent in acute myeloblastic leukemias (AMLs) and in therapy-related myelodysplastic syndromes, but rarely in acute lymphoblastic leukemias (ALLs) and chronic myelogenous leukemias (CMLs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_provenance.
- NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_assertion evidence source_evidence_literature NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_provenance.
- NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_assertion SIO_000772 18202228 NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_provenance.
- NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_assertion wasDerivedFrom befree-2016 NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_provenance.
- NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_assertion wasGeneratedBy ECO_0000203 NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_provenance.
- befree-2016 importedOn "2016-02-19" NP650502.RAkYaZvYwLqjFknN6a0RxO1h8zhNh_IYZ3Lse-c-ynGOI130_provenance.