@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY> .
@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 dcterms: <http://purl.org/dc/terms/> .
@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:NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY130_head {
  this: np:hasAssertion dgn-np:NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY130_assertion;
    np:hasProvenance dgn-np:NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY130_provenance;
    np:hasPublicationInfo dgn-np:NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY130_provenance a np:Provenance .
  
  dgn-np:NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY130_assertion {
  miriam-gene:8718 a ncit:C16612 .
  
  lld:C0014378 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY130_provenance {
  dgn-np:NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY130_assertion dcterms:description
      "[Our aim was to test whether these type 1 diabetes-associated IFIH1 polymorphisms are associated with the occurrence of enterovirus infection in the gut of healthy children, or influence the lack of association between gut enterovirus infection and islet autoimmunity.After testing of 46,939 Norwegian newborns, 421 children carrying the high risk genotype for type 1 diabetes (HLA-DR4-DQ8/DR3-DQ2) as well as 375 children without this genotype were included for monthly fecal collections from 3 to 35 months of age, and genotyped for the IFIH1 polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP326272.RACNZYL_LQVkDrBi6fVX5Ge647D5LBPYPrrJGTAGDnVqY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:10+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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