Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_provenance.
- NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_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." NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_provenance.
- NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_assertion evidence source_evidence_literature NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_provenance.
- NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_assertion SIO_000772 21742036 NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_provenance.
- NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_assertion wasDerivedFrom befree-2016 NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_provenance.
- NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_assertion wasGeneratedBy ECO_0000203 NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_provenance.
- befree-2016 importedOn "2016-02-19" NP908386.RAvFzLUve3GXN0U1eWAO25Jn4fup_DhJ3AxsHDwRIkTV4130_provenance.