Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance.
- NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_assertion description "[The majority of genes identified by RDA showed nearly complete concordance with microarray results, and also led to the identification of some differentially expressed genes such as lysyl oxidase, copper transporter ATP7A, EphB6, RUNX2 and a variant of RUNX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance.
- NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_assertion evidence source_evidence_literature NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance.
- NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_assertion SIO_000772 16314837 NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance.
- NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_assertion wasDerivedFrom befree-20140225 NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance.
- NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_assertion wasGeneratedBy ECO_0000203 NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP876871.RAdeNoY-qVsK2EiHachXd8HasBEaCYDa3iXHKKuKiKPbQ130_provenance.