Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_provenance.
- NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_assertion description "[RUNX1 mutations clustered in the intermediate-risk cytogenetic group (46 of 640, 7.2%; cytogenetically normal, 34 of 538, 6.3%), whereas they were less frequent in adverse-risk cytogenetics (five of 109, 4.6%) and absent in core-binding-factor AML (0 of 77) and acute promyelocytic leukemia (0 of 61).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_provenance.
- NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_assertion evidence source_evidence_literature NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_provenance.
- NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_assertion SIO_000772 21343560 NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_provenance.
- NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_assertion wasDerivedFrom befree-2016 NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_provenance.
- NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_assertion wasGeneratedBy ECO_0000203 NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_provenance.
- befree-2016 importedOn "2016-02-19" NP874344.RAF4lJXYSSDC1Hx2_bEcd9CRoHRvDeeZCoIqDi228Ung0130_provenance.