Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_assertion> ?p ?o ?g. }
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- NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_assertion type Assertion NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_head.
- NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_assertion description "[We found clustering of rare variants of the POLG1 CAG-repeat, encoding a polyglutamine tract, in Finnish patients with idiopathic PD as compared to their spouses (p = 0.003; OR 3.01, 95% CI 1.35 to 6.71), population controls (p = 0.001; OR 2.45, 95% CI 1.45 to 4.14), and patients with nonparkinsonian neurologic disorders (p = 0.05, OR 1.98, 95% CI 0.97 to 4.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_provenance.
- NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_assertion evidence source_evidence_literature NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_provenance.
- NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_assertion SIO_000772 17846414 NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_provenance.
- NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_assertion wasDerivedFrom befree-20150227 NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_provenance.
- NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_assertion wasGeneratedBy ECO_0000203 NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_provenance.