Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_provenance.
- NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_assertion description "[Here, they evaluated if NCSTN polymorphisms increased risk of AD in the eastern Finnish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_provenance.
- NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_assertion evidence source_evidence_literature NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_provenance.
- NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_assertion SIO_000772 15249634 NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_provenance.
- NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_assertion wasDerivedFrom befree-20150227 NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_provenance.
- NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_assertion wasGeneratedBy ECO_0000203 NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP871382.RAQ2hododgHI7KCoJrzl2W1BBxXMXA-9Al8WEer0zXFkY130_provenance.