Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_provenance.
- NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_assertion description "[Lafora disease (LD) is the inherited progressive myoclonus epilepsy caused by mutations in either EPM2A gene, encoding the protein phosphatase laforin or the NHLRC1 gene, encoding the ubiquitin ligase malin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_provenance.
- NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_assertion evidence source_evidence_literature NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_provenance.
- NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_assertion SIO_000772 21742036 NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_provenance.
- NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_assertion wasDerivedFrom befree-20140225 NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_provenance.
- NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_assertion wasGeneratedBy ECO_0000203 NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP407682.RAcIfndyeUI7zl2degJJt9L9WUW3lWlxro07E2rw-lmoo130_provenance.