Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_provenance.
- NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_assertion description "[A rare variant (AL746Thr) of the ATP13A2 was associated with an increased risk of Parkinson disease among ethnic Chinese in Asia/studies are needed to clarify the functional role of this genetic risk factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_provenance.
- NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_assertion evidence source_evidence_literature NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_provenance.
- NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_assertion SIO_000772 19015489 NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_provenance.
- NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_assertion wasDerivedFrom lhgdn-20090331 NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_provenance.
- NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_assertion wasGeneratedBy ECO_0000203 NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP243744.RAz4DZGn0NqqHIHVvKA9DiVXudj6HXgmC4F4ZyZbPAX7c130_provenance.