Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_provenance.
- NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_assertion description "[To determine whether the frequency of dopamine receptor genetic variants and APOE alleles in patients with PD with and without chronic visual hallucinations resembles the pattern previously documented in patients with Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_provenance.
- NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_assertion evidence source_evidence_literature NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_provenance.
- NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_assertion SIO_000772 11176958 NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_provenance.
- NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_assertion wasDerivedFrom befree-2016 NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_provenance.
- NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_assertion wasGeneratedBy ECO_0000203 NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP307232.RAiqkl9Lglg0WY2ORVZaCBB3wIw5BDDf1CkdC00PuOHkQ130_provenance.