Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_provenance.
- NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_assertion description "[The 6055G>A mutation in the leucine-rich repeat kinase 2 (LRRK2) gene results in a G2019S substitution in the mixed-lineage kinase domain of Lrrk2, causing autosomal dominant Parkinson's disease (PD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_provenance.
- NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_assertion evidence source_evidence_literature NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_provenance.
- NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_assertion SIO_000772 17385669 NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_provenance.
- NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_assertion wasDerivedFrom befree-20140225 NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_provenance.
- NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_assertion wasGeneratedBy ECO_0000203 NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP777242.RAWQNHmjz1r3RHyorD_MAZrzsCdXuOalnnNMXfoHtieYE130_provenance.