Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_provenance.
- NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_assertion wasGeneratedBy ECO_0000203 NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_provenance.
- NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_assertion wasDerivedFrom befree-20150227 NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_provenance.
- NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_assertion SIO_000772 17057786 NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_provenance.
- NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_assertion evidence source_evidence_literature NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_provenance.
- NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_assertion description "[hOgg1 326C allele frequency was 21.35% (38 of 178) in the AMD group compared with 19.12% (65 of 340) in the random controls and 19.59% (38 of 194) in the age-matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602216.RAgpJmDZg8Y_ykya58Xg6xHU0d8AwfrKo0ERpM1PhLyLs130_provenance.