Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_provenance.
- NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_assertion description "[These results suggest that JMML with PTPN11 mutation might be a distinct subgroup with specific clinical characteristics and poor outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_provenance.
- NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_assertion evidence source_evidence_literature NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_provenance.
- NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_assertion SIO_000772 19047918 NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_provenance.
- NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_assertion wasDerivedFrom gad-20130706 NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_provenance.
- NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_assertion wasGeneratedBy ECO_0000203 NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_provenance.
- gad-20130706 importedOn "2013-07-06" NP67753.RAmYJGtfxC_omxXKmDTWUBZbI3FwgH703esDb6L27OY0A130_provenance.