@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_head {
   this: np:hasAssertion dgn-np:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_assertion ;
    np:hasProvenance dgn-np:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_provenance ;
    np:hasPublicationInfo dgn-np:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_assertion a np:Assertion .
  dgn-np:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_provenance a np:Provenance .
  dgn-np:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_assertion {
   miriam-gene:3976 a ncit:C16612 .
  lld:C0026769 a ncit:C7057 .
  dgn-gda:DGNfda9c75a9c844c30a008d75daf98830d sio:SIO_000628 miriam-gene:3976 , lld:C0026769 ;
    a sio:SIO_001122 .
}
dgn-np:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_provenance {
   dgn-np:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_assertion dct:description "[The results indicate that the LIF 3' UTR StuI polymorphism is not associated with multiple sclerosis, however we cannot exclude the hypothesis that other polymorphic alleles of LIF could be implicated in MS susceptibility.]. 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:19251277 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP70351.RAfNF_iSC_n4RBb_tZetQjin0VF4d0bSYA6QRHWTFuc4w130_publicationInfo {
   this: dct:created "2014-10-02T12:32:34+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}