Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_provenance.
- NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_assertion description "[The existence of common genomic alterations in basal-like, ERBB2 and luminal B breast tumours may suggest a common cell origin or clonal selection of these tumour subtypes, arising from an ER-negative CSC or from a progenitor cell (PC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_provenance.
- NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_assertion evidence source_evidence_literature NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_provenance.
- NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_assertion SIO_000772 18596026 NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_provenance.
- NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_assertion wasDerivedFrom befree-2016 NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_provenance.
- NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_assertion wasGeneratedBy ECO_0000203 NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_provenance.
- befree-2016 importedOn "2016-02-19" NP679903.RANFL_iMeZ1E6VWavOXj-QqlsGz-5kIpYjCmCLrt-YM3U130_provenance.