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- source_evidence_literature type ECO_0000212 NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP633477.RAZdtlBW0rMMVf8E4ciN5CH9mTcnlwloe3mtAfHSTrGSA130_provenance.