Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_provenance.
- NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_assertion description "[CFH CC genotype was strongly associated with late neovascular AMD (OR, 6.0; 95% confidence interval [CI], 1.5-23.5) but not with late atrophic AMD (OR, 0.9; 95% CI, 0.2-4.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_provenance.
- NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_assertion evidence source_evidence_literature NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_provenance.
- NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_assertion SIO_000772 21642625 NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_provenance.
- NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_assertion wasDerivedFrom befree-2016 NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_provenance.
- NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_assertion wasGeneratedBy ECO_0000203 NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_provenance.
- befree-2016 importedOn "2016-02-19" NP899542.RAYqdk4a38dqX-W0yFSAooPqUA9N0RkyU4zyrLl64rnbA130_provenance.