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- source_evidence_literature type ECO_0000212 NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_provenance.
- NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_assertion description "[Several of these variants are in or near genes with a biological rationale for conferring EOC risk, including ZFP36L1 and RAD51B for mucinous EOC (rs17106154, OR�=�1.17, P�=�0.029, n�=�1,483 cases), GRB10 for endometrioid and clear cell EOC (rs2190503, P�=�0.014, n�=�2,903 cases), and C22orf26/BPIL2 for LMP serous EOC (rs9609538, OR�=�0.86, P�=�0.0043, n�=�892 cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_provenance.
- NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_assertion evidence source_evidence_literature NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_provenance.
- NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_assertion SIO_000772 24190013 NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_provenance.
- NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_assertion wasDerivedFrom befree-2016 NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_provenance.
- NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_assertion wasGeneratedBy ECO_0000203 NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1124917.RAa-S5QgecIYmqD06UrY4fIQ80XqudfLJn_yi5NRHThwI130_provenance.