@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_head { this: np:hasAssertion dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_assertion; np:hasProvenance dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_provenance; np:hasPublicationInfo dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_publicationInfo; a np:Nanopublication . dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_assertion a np:Assertion . dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_provenance a np:Provenance . dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_publicationInfo a np:PublicationInfo . } dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_assertion { miriam-gene:6775 a ncit:C16612 . lld:C0010346 a ncit:C7057 . dgn-gda:DGNaa015eb8c9e9e0983cc028a0648b3ba2 sio:SIO_000628 miriam-gene:6775, lld:C0010346; a sio:SIO_001121 . } dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_provenance { dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_assertion dcterms:description "[Our meta-analysis revealed that the STAT4 rs7574865 polymorphism is associated with four autoimmune diseases with systemic pathology, including systemic lupus erythematosus (OR = 1.52; 95% CI = 1.48 - 1.56, P<1.0 × 10(-16)), rheumatoid arthritis (OR = 1.27; 95% CI = 1.21 - 1.33, P < 1.00 × 10(-16)), systemic sclerosis (OR = 1.38; 95% CI = 1.27 - 1.50, P < 1.44 × 10(-14)), and primary Sjogren's syndrome (OR = 1.32; 95% CI = 1.01 - 1.73, P = 4.40 × 10(-2)), while no association was found with type I diabetes, juvenile idiopathic arthritis, ulcerative colitis and Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:23628400; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP727941.RAVL3w1pASA71vM-rkAOJNnjy9YwhVmdxP_MWgb-P0LsU130_publicationInfo { this: dcterms:created "2014-10-02T12:39:22+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }