Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_assertion> ?p ?o ?g. }
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- NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_assertion type Assertion NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_head.
- NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_assertion description "[Recessively inherited deletions/duplications and point mutations in the parkin gene are the most common cause of early-onset parkinsonism known so far, but in an increasing number of studies, genetic variations in the serine/threonine kinase domain of the PINK1 gene are found to explain early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_provenance.
- NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_assertion evidence source_evidence_literature NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_provenance.
- NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_assertion SIO_000772 19087301 NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_provenance.
- NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_assertion wasDerivedFrom befree-2016 NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_provenance.
- NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_assertion wasGeneratedBy ECO_0000203 NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_provenance.