Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_provenance.
- NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_assertion description "[Targeted disruption of FANCC and FANCG in human cancer provides a preclinical model for specific therapeutic options.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_provenance.
- NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_assertion evidence source_evidence_literature NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_provenance.
- NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_assertion SIO_000772 16762635 NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_provenance.
- NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_assertion wasDerivedFrom befree-20150227 NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_provenance.
- NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_assertion wasGeneratedBy ECO_0000203 NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP394602.RAd6NF1eYF4wAzg-9ld47lwp5r7uHBxjdGh17JiXpnDL0130_provenance.