Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_provenance.
- NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_assertion description "[A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_provenance.
- NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_assertion evidence source_evidence_literature NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_provenance.
- NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_assertion SIO_000772 16633828 NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_provenance.
- NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_assertion wasDerivedFrom gad-20150221 NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_provenance.
- NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_assertion wasGeneratedBy ECO_0000203 NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP100190.RAVxveWe9M3B9vEyHm6TwFMvx5qIdEanXhS5m_eEbwTOw130_provenance.