Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance.
- NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance.
- NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_assertion evidence source_evidence_literature NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance.
- NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_assertion SIO_000772 12402271 NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance.
- NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_assertion wasDerivedFrom befree-20140225 NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance.
- NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_assertion wasGeneratedBy ECO_0000203 NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP792903.RAA1uFoXg6Ewjp7lTy170NLx99ujpF9O7yZxBGLAJ8cVY130_provenance.