Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance.
- NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_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." NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance.
- NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_assertion evidence source_evidence_literature NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance.
- NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_assertion SIO_000772 18571946 NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance.
- NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_assertion wasDerivedFrom befree-20150227 NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance.
- NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_assertion wasGeneratedBy ECO_0000203 NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance.