Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_provenance.
- NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_assertion description "[IL1RN 2R/2R genotype [odds ratio (OR) 2.43; 95% confidence interval (CI) 1.19-4.96] and allele IL1RN Ex5-35C were associated with an increased risk of Hp(+) non-cardia GC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_provenance.
- NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_assertion evidence source_evidence_literature NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_provenance.
- NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_assertion SIO_000772 18628242 NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_provenance.
- NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_assertion wasDerivedFrom befree-2016 NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_provenance.
- NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_assertion wasGeneratedBy ECO_0000203 NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_provenance.
- befree-2016 importedOn "2016-02-19" NP682245.RAxFMZhtPL4ItDF0fFJxxy3qmIjz9v_0h-1d9qFAJ8Vhc130_provenance.