Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_provenance.
- NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_assertion description "[Inactivation of RUNX3 was observed in 70% of the adenocarcinoma samples, and this was associated with promoter hypermethylation but not biased to EGFR/KRAS mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_provenance.
- NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_assertion evidence source_evidence_literature NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_provenance.
- NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_assertion SIO_000772 22729835 NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_provenance.
- NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_assertion wasDerivedFrom befree-20140225 NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_provenance.
- NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_assertion wasGeneratedBy ECO_0000203 NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783219.RAsw026CV2PlkE0Dk145t2GNTO3I19XDYyumcZVEKq8Qg130_provenance.