Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_provenance.
- NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_assertion description "[Polymorphisms in NQO1, IL-10 and PTPN11, in combination with HP status, could be used to identify individuals who are more likely to develop IM and therefore GC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_provenance.
- NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_assertion evidence source_evidence_literature NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_provenance.
- NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_assertion SIO_000772 19822020 NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_provenance.
- NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_assertion wasDerivedFrom befree-20140225 NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_provenance.
- NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_assertion wasGeneratedBy ECO_0000203 NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP329579.RAI1vQf_Twp-CmqWjOtw3FdB57cg1aKzh2dS9lsKqR3cA130_provenance.