Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_provenance.
- NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_assertion description "[Mutations of parkin, an E3 ubiquitin ligase that strongly binds to microtubules, are the most frequent cause of recessively inherited PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_provenance.
- NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_assertion evidence source_evidence_literature NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_provenance.
- NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_assertion SIO_000772 25332110 NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_provenance.
- NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_assertion wasDerivedFrom befree-2016 NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_provenance.
- NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_assertion wasGeneratedBy ECO_0000203 NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1230988.RAwzz-C1mpoIw-6TpjzmRw-xoPm4ypL8l2tARshs5wOOw130_provenance.