Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance.
- NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_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." NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance.
- NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_assertion evidence source_evidence_literature NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance.
- NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_assertion SIO_000772 12402271 NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance.
- NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_assertion wasDerivedFrom befree-20140225 NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance.
- NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_assertion wasGeneratedBy ECO_0000203 NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP205886.RA_cuR9CWy303BZcnjOSy33l66C4t47kee_X8_4wEXMVk130_provenance.