Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_provenance.
- NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_assertion description "[The ecNOS gene a/b polymorphism and the NADH/NADPH oxidase p22 phox gene C242T polymorphism were found to be significantly associated with the development of CAD in Korean male patients less than 51 years old.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_provenance.
- NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_assertion evidence source_evidence_literature NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_provenance.
- NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_assertion SIO_000772 11530961 NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_provenance.
- NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_assertion wasDerivedFrom gad-20150221 NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_provenance.
- NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_assertion wasGeneratedBy ECO_0000203 NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_provenance.
- gad-20150221 importedOn "2015-02-21" NP55803.RAiFm3LRobFU0BZFWucT8G1MKHrlvg4-Xft1FZk-xb02s130_provenance.