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- source_evidence_literature type ECO_0000212 NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_provenance.
- NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_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." NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_provenance.
- NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_assertion evidence source_evidence_literature NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_provenance.
- NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_assertion SIO_000772 16971227 NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_provenance.
- NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_assertion wasDerivedFrom befree-2016 NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_provenance.
- NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_assertion wasGeneratedBy ECO_0000203 NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_provenance.
- befree-2016 importedOn "2016-02-19" NP569197.RA_BuJUd5xk6anKNfElLccqENHyQm2IgCaIr9yaDt4GqE130_provenance.