Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_provenance.
- NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_assertion description "[Patients with FAB M0 and M7 AML (no MPO expression) or M3 AML (100% MPO expression) and Down's syndrome were excluded.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_provenance.
- NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_assertion evidence source_evidence_literature NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_provenance.
- NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_assertion SIO_000772 17763467 NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_provenance.
- NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_assertion wasDerivedFrom befree-20140225 NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_provenance.
- NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_assertion wasGeneratedBy ECO_0000203 NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP190404.RA7QNn4x_L1KrTOqVsvPXaepwnIsP-Hwo29be5wf3tsPs130_provenance.