Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_provenance.
- NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_assertion wasGeneratedBy ECO_0000203 NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_provenance.
- NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_assertion wasDerivedFrom befree-20150227 NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_provenance.
- NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_assertion SIO_000772 19808697 NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_provenance.
- NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_assertion evidence source_evidence_literature NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_provenance.
- NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_assertion description "[Somatic mutation of the AML1/RUNX1(RUNX1) gene is seen in acute myeloid leukemia (AML) M0 subtype and in AML transformed from myelodysplastic syndrome, but the impact of this gene mutation on survival in AML patients remains unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285488.RAaT1qMkyfOOsftyVw3Dv2gDeE0bf1PSuEvFiS8f2u-qQ130_provenance.