Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_provenance.
- NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_assertion description "[We identified 13 common genes (ADARB2, CEACAM6, CNTNAP2, COL19A1, DEF4, DRAXIN, FCER2, HBG1, NCAPG2, PVRL2, SLC2A14, SNCA, and TCL1B) showing significant differential expression between G2019S-associated PD and asymptomatic carriers and also between idiopathic PD and controls but not between untreated and treated patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_provenance.
- NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_assertion evidence source_evidence_literature NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_provenance.
- NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_assertion SIO_000772 25475535 NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_provenance.
- NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_assertion wasDerivedFrom befree-2016 NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_provenance.
- NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_assertion wasGeneratedBy ECO_0000203 NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244862.RA7bOz9uxb_IaRIN9eCHfdB53qWYoErH7jlMVzDLvLiK4130_provenance.