Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance.
- NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_assertion description "[Increased incidence of p53 gene aberrations or chromosome 17p monosomy resulting from an isochromosome 17q [i(17q)] has been observed with transition of chronic myelogenous leukemia (CML) to myeloid blast crisis (BC), and in some patients with poor risk acute myeloid leukemia (AML) progressing from myelodysplastic syndrome (MDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance.
- NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_assertion evidence source_evidence_literature NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance.
- NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_assertion SIO_000772 8505851 NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance.
- NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_assertion wasDerivedFrom befree-20140225 NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance.
- NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_assertion wasGeneratedBy ECO_0000203 NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance.