Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_provenance.
- NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_assertion description "[We found that carriers of the C allele of a polymorphism in the 3'-UTR of COX2 had a significantly increased risk of lung cancer, with odds ratios of 4.28 (95% CI, 2.44-7.49) for homozygotes and 2.12 (95% CI, 1.25-3.59) for heterozygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_provenance.
- NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_assertion evidence source_evidence_literature NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_provenance.
- NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_assertion SIO_000772 14604894 NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_provenance.
- NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_assertion wasDerivedFrom befree-20140225 NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_provenance.
- NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_assertion wasGeneratedBy ECO_0000203 NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP620797.RA-NQmT-0F9nuethkK8xhO9VVlPlltM8Yf_8US7MCcnbU130_provenance.