Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_provenance.
- NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_assertion wasGeneratedBy ECO_0000203 NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_provenance.
- NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_assertion wasDerivedFrom befree-20140225 NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_provenance.
- NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_assertion SIO_000772 19110536 NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_provenance.
- NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_assertion evidence source_evidence_literature NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_provenance.
- NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_assertion description "[In up to 8010 cases and 9733 controls we found some evidence for an association with T1D in the regions containing genes: 2q32/STAT4, 17q21/STAT3, 5p15/ERAP1 (ARTS1), 6q23/TNFAIP3 and 12q13/KIF5A/PIP4K2C with allelic P-values ranging from 3.70 x 10(-3) to 3.20 x 10(-5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP623160.RAsmpm5_nx7apkkU7Wjq3A1PxLMDot9RpGS0SBhlLj5_A130_provenance.