Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance.
- NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_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." NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance.
- NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_assertion evidence source_evidence_literature NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance.
- NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_assertion SIO_000772 18571946 NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance.
- NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_assertion wasDerivedFrom befree-20150227 NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance.
- NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_assertion wasGeneratedBy ECO_0000203 NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance.
- befree-20150227 importedOn "2015-02-27" NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance.