Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance.
- NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_assertion description "[However, individuals with AATD phenotypes had a higher risk of developing squamous cell lung cancer then those with non-deficient AAT variants (OR = 4.51, 95% CI = 1.66-12.29).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance.
- NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_assertion evidence source_evidence_literature NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance.
- NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_assertion SIO_000772 16971227 NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance.
- NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_assertion wasDerivedFrom gad-20130706 NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance.
- NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_assertion wasGeneratedBy ECO_0000203 NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66478.RAqXcav71GOeD4tTrcXeiuiu8q0gcR_tzbehpUXYbHJ8A130_provenance.