Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_provenance.
- NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_assertion description "[The K allele was significantly more frequent in FH subjects without premature CHD than in FH subjects with premature CHD suggesting that the genetic variant R219K in ABCA1 could influence the development and progression of atherosclerosis in FH subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_provenance.
- NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_assertion evidence source_evidence_literature NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_provenance.
- NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_assertion SIO_000772 12624133 NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_provenance.
- NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_assertion wasDerivedFrom lhgdn-20090331 NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_provenance.
- NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_assertion wasGeneratedBy ECO_0000203 NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198559.RAcGCT3FCRxIWsh9BrU6JT01F2pBhBySGAQal_d8O-tCM130_provenance.