Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_provenance.
- NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_assertion description "[The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_provenance.
- NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_assertion evidence source_evidence_literature NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_provenance.
- NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_assertion SIO_000772 18411254 NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_provenance.
- NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_assertion wasDerivedFrom befree-20150227 NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_provenance.
- NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_assertion wasGeneratedBy ECO_0000203 NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP976673.RA7fyaV8M1kWi3y6A6Bgaf4tal6BdgY3RbFnVNjv155hQ130_provenance.