@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8> .
@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:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_head {
  this: np:hasAssertion dgn-np:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_assertion;
    np:hasProvenance dgn-np:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_provenance;
    np:hasPublicationInfo dgn-np:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_assertion a np:Assertion .
  
  dgn-np:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_provenance a np:Provenance .
  
  dgn-np:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_assertion {
  miriam-gene:3106 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGNc4ea638d0389275cb2e5d85c1148e704 sio:SIO_000628 miriam-gene:3106, lld:C0024141;
    a sio:SIO_001121 .
}

dgn-np:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_provenance {
  dgn-np:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_assertion dcterms:description
      "[In this study, we tested 17 single nucleotide polymorphisms (SNP) from 16 gene regions that have been reported in several autoimmune diseases including rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), multiple sclerosis (MS), ankylosing spondylitis (AS) and Crohn's disease (CD) to determine whether the variants are also associated with type 1 diabetes (T1D).]. 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:19110536;
    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:NP665655.RATDb0MRXKVuhwN5zd99VvN20H45PxCmqOd03dVfk9pA8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:42+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}