Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_provenance.
- NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_assertion description "[FGG + FGA haplotype 3 (H3) was associated with an increased risk of ischemic stroke (odds ratio [OR] 1.36, 95% confidence interval [CI] 1.09-1.69) and the risk estimate for hemorrhagic stroke was 0.71 (95% CI 0.46-1.09) compared to the most frequent H1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_provenance.
- NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_assertion evidence source_evidence_literature NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_provenance.
- NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_assertion SIO_000772 18690352 NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_provenance.
- NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_assertion wasDerivedFrom befree-2016 NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_provenance.
- NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_assertion wasGeneratedBy ECO_0000203 NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_provenance.
- befree-2016 importedOn "2016-02-19" NP686783.RAKqX7t4BM3Mw7Gc-a1LNvPL3SLdme-atmVGupc9bQ7VU130_provenance.