Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_assertion> ?p ?o ?g. }
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- NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_assertion type Assertion NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_head.
- NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_assertion description "[Parkinson protein 2, E3 ubiquitin protein ligase (PARK2) gene mutations are the most frequent causes of autosomal recessive early onset Parkinson's disease and juvenile Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_provenance.
- NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_assertion evidence source_evidence_literature NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_provenance.
- NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_assertion SIO_000772 25136611 NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_provenance.
- NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_assertion wasDerivedFrom befree-2016 NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_provenance.
- NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_assertion wasGeneratedBy ECO_0000203 NP1211886.RAp7lSPqXADlKoCmEJU6yV8fIMmdPKmOEf4xQ64MBBl9M130_provenance.