Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance.
- NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_assertion description "[Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder with myoclonic jerks and dystonic contractions most frequently due to a mutation in the epsilon-sarcoglycan (SGCE, DYT11) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance.
- NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_assertion evidence source_evidence_literature NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance.
- NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_assertion SIO_000772 18571946 NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance.
- NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_assertion wasDerivedFrom befree-20140225 NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance.
- NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_assertion wasGeneratedBy ECO_0000203 NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance.