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- source_evidence_literature type ECO_0000212 NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_provenance.
- NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_assertion description "[RUNX1 gene alterations are associated with acquired and inherited hematologic malignancies that include familial platelet disorder/acute myeloid leukemia, primary or secondary acute myeloid leukemia, and chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_provenance.
- NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_assertion evidence source_evidence_literature NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_provenance.
- NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_assertion SIO_000772 22677128 NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_provenance.
- NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_assertion wasDerivedFrom befree-2016 NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_provenance.
- NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_assertion wasGeneratedBy ECO_0000203 NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_provenance.
- befree-2016 importedOn "2016-02-19" NP988088.RAtHrSiNZHXYYDDnklJDIwkfmPCypb1Me-4DVQSVGIttI130_provenance.