Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_assertion> ?p ?o ?g. }
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- NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_assertion type Assertion NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_head.
- NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_assertion description "[Loss-of-function mutations in PARK2, the gene encoding the E3 ubiquitin ligase Parkin, are the most frequent cause of recessive Parkinson's disease (PD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_provenance.
- NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_assertion evidence source_evidence_literature NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_provenance.
- NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_assertion SIO_000772 24852371 NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_provenance.
- NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_assertion wasDerivedFrom befree-2016 NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_provenance.
- NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_assertion wasGeneratedBy ECO_0000203 NP1184601.RAuJckutl12_4gklAe3nmVbPlPEkZdICrNMFraI43cTjM130_provenance.