Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_provenance.
- NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_assertion wasGeneratedBy ECO_0000203 NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_provenance.
- NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_assertion wasDerivedFrom befree-20150227 NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_provenance.
- NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_assertion SIO_000772 21742036 NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_provenance.
- NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_assertion evidence source_evidence_literature NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_provenance.
- NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_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." NP988828.RABzqTQk_fHANLb9r-PJztjRUFQIK5pKK6IxztJP35aOM130_provenance.