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- source_evidence_literature type ECO_0000212 NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_provenance.
- NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_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." NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_provenance.
- NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_assertion evidence source_evidence_literature NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_provenance.
- NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_assertion SIO_000772 19822020 NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_provenance.
- NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_assertion wasDerivedFrom befree-2016 NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_provenance.
- NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_assertion wasGeneratedBy ECO_0000203 NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_provenance.
- befree-2016 importedOn "2016-02-19" NP768878.RARFRI-rSLKNFneAbA7-B9SjJ_1IgFEJUhbz8V3b0C2D4130_provenance.