Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_provenance.
- NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_assertion wasGeneratedBy ECO_0000203 NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_provenance.
- NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_assertion wasDerivedFrom befree-20150227 NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_provenance.
- NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_assertion SIO_000772 19110536 NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_provenance.
- NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_assertion evidence source_evidence_literature NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_provenance.
- NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_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." NP717306.RAVnIn38TGu8-iNxrps8lPr7TLxY7o3MflfOLEXq-s6jQ130_provenance.