@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU> .
@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:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_head {
  this: np:hasAssertion dgn-np:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_assertion;
    np:hasProvenance dgn-np:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_provenance;
    np:hasPublicationInfo dgn-np:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_assertion a np:Assertion .
  
  dgn-np:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_provenance a np:Provenance .
  
  dgn-np:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_assertion {
  miriam-gene:6696 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN41cb5168a719b77569df37bac7b7d4ee sio:SIO_000628 miriam-gene:6696, lld:C0026769;
    a sio:SIO_001121 .
}

dgn-np:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_provenance {
  dgn-np:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_assertion dcterms:description
      "[The aim of this study was to investigate the role of OPN genes in the pathogenesis of MS. Polymorphisms at the 8090th, 9250th and 9583rd positions in OPN were detected by PCR-RFLP from DNAs of 116 MS Japanese patients and 124 healthy controls.]. 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:12620651;
    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:NP480266.RAYmcKF6r-s4a-LlW7T4Yv6qLW0fDocN8KBB5CT0NP8OU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:47+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" .
}