Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance.
- NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_assertion description "[Dyschromatosis symmetrica hereditaria (DSH) is an autosomal dominant pigmentary genodermatosis characterized by hyperpigmented and hypopigmented macules of on the extremities and caused by the mutations in the ADAR gene(also called DSRAD) encoding for RNA-specific adenosine deaminase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance.
- NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_assertion evidence source_evidence_literature NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance.
- NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_assertion SIO_000772 15146470 NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance.
- NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_assertion wasDerivedFrom befree-2016 NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance.
- NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_assertion wasGeneratedBy ECO_0000203 NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance.
- befree-2016 importedOn "2016-02-19" NP444351.RAQdHdtmSVn7VXHCOq6WE8NGvWEUVQY-tXJzgKQU-t50A130_provenance.