Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_provenance.
- NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_assertion description "[Unverricht-Lundborg disease (ULD), progressive myoclonic epilepsy type 1 (EPM1, OMIM254800), is an autosomal recessively inherited neurodegenerative disorder characterized by age of onset from 6 to 16 years, stimulus-sensitive myoclonus, and tonic-clonic epileptic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_provenance.
- NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_assertion evidence source_evidence_literature NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_provenance.
- NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_assertion SIO_000772 18325013 NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_provenance.
- NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_assertion wasDerivedFrom befree-2016 NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_provenance.
- NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_assertion wasGeneratedBy ECO_0000203 NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_provenance.
- befree-2016 importedOn "2016-02-19" NP659274.RAf4IQNH9PNv66RRqoGe7vDS32dyAB0HwhNT2-76vBqI8130_provenance.