Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_provenance.
- NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_assertion description "[Nucleotide sequencing of the highly conserved SMPD3 gene in a large panel of human cancers revealed mutations in 5 (5%) of 92 acute myeloid leukemias (AMLs) and 8 (6%) of 131 acute lymphoid leukemias (ALLs), but not in other tumor types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_provenance.
- NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_assertion evidence source_evidence_literature NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_provenance.
- NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_assertion SIO_000772 18299447 NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_provenance.
- NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_assertion wasDerivedFrom befree-20140225 NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_provenance.
- NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_assertion wasGeneratedBy ECO_0000203 NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP923221.RAWtWYaSL_aJpypFNHhhSbOQMXaEOEgwfypOLLg-X0MWY130_provenance.