@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8> .
@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:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_head {
  this: np:hasAssertion dgn-np:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_assertion;
    np:hasProvenance dgn-np:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_provenance;
    np:hasPublicationInfo dgn-np:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_assertion a np:Assertion .
  
  dgn-np:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_provenance a np:Provenance .
  
  dgn-np:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_assertion {
  miriam-gene:6696 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN7a410634e197c9a6780144816837aeeb sio:SIO_000628 miriam-gene:6696, lld:C0003873;
    a sio:SIO_001121 .
}

dgn-np:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_provenance {
  dgn-np:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_assertion dcterms:description
      "[Our data suggest that, unlike the reported effect of the OPN SNP conferring predisposition to common diseases such as multiple sclerosis or systemic lupus erythematosus, these OPN gene polymorphisms do not contribute to RA susceptibility in the Spanish population we studied.]. 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:15742429;
    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:NP200409.RAMYXEGn8t6eiravh7bKyyjHfgios3GeVHe0Frsq3wBU8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:50+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" .
}