Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_provenance.
- NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_assertion description "[We have carried out a high-resolution array CGH and expression profiling on 25 ES tumour samples to characterize the DNA copy number aberrations (CNA) occurring in these tumours and determine their association with gene-expression profiles and clinical outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_provenance.
- NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_assertion evidence source_evidence_literature NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_provenance.
- NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_assertion SIO_000772 17952124 NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_provenance.
- NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_assertion wasDerivedFrom befree-2016 NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_provenance.
- NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_assertion wasGeneratedBy ECO_0000203 NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP636614.RAk5g-tnnD2d62ZVvgNLtI6-Cjd6tsvZbI-Swxav_6wJ4130_provenance.