Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_provenance.
- NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_assertion description "[Mutations in the ATP-binding cassette transporter ABCA1 underlie Tangier disease and familial hypoalphaliproteinemia (FHA), disorders that are characterised by reduced high-density lipoprotein-cholesterol (HDL-C) concentration and cholesterol efflux, and increased coronary artery disease (CAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_provenance.
- NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_assertion evidence source_evidence_literature NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_provenance.
- NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_assertion SIO_000772 12709788 NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_provenance.
- NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_assertion wasDerivedFrom befree-2016 NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_provenance.
- NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_assertion wasGeneratedBy ECO_0000203 NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_provenance.
- befree-2016 importedOn "2016-02-19" NP392014.RAIFsjCKFWgs_CVk0w27UbPsXqHI1isDGNFzFsGbkfObU130_provenance.