Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_provenance.
- NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_assertion description "[We conclude that the identified polymorphic sites in the human NURR1 are unlikely to be involved in conferring susceptibility for SZ or PD in our patient material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_provenance.
- NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_assertion evidence source_evidence_literature NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_provenance.
- NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_assertion SIO_000772 12815740 NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_provenance.
- NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_assertion wasDerivedFrom befree-20140225 NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_provenance.
- NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_assertion wasGeneratedBy ECO_0000203 NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP502387.RAvTSWnUkICwq5cRGTDzbU7bJ6iS8jNzeZFr4bEFYdkgM130_provenance.