@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk> .
@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:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_head {
  this: np:hasAssertion dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_assertion;
    np:hasProvenance dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_provenance;
    np:hasPublicationInfo dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_assertion a np:Assertion .
  
  dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_provenance a np:Provenance .
  
  dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_assertion {
  miriam-gene:5698 a ncit:C16612 .
  
  lld:C0003864 a ncit:C7057 .
  
  dgn-gda:DGN3785d91e0641dd03fd7f3b82938792d5 sio:SIO_000628 miriam-gene:5698, lld:C0003864;
    a sio:SIO_001121 .
}

dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_provenance {
  dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_assertion dcterms:description
      "[Our data is thus internally consistent in demonstrating no association between LMP2 genotypes and either disease severity or peripheral arthritis, and supports the notion that polymorphism of LMP2 primarily influences the development of AAU and not some other phenotype of AS.]. 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:9348140;
    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:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:50+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" .
}