@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg> .
@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:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_head {
  this: np:hasAssertion dgn-np:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_assertion;
    np:hasProvenance dgn-np:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_provenance;
    np:hasPublicationInfo dgn-np:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_assertion a np:Assertion .
  
  dgn-np:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_provenance a np:Provenance .
  
  dgn-np:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_assertion {
  miriam-gene:7190 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN2dcd74c21f1ac1af8d7a021d9118cd1a sio:SIO_000628 miriam-gene:7190, lld:C0003873;
    a sio:SIO_001121 .
}

dgn-np:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_provenance {
  dgn-np:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_assertion dcterms:description
      "[These data suggest that the 65kD HSP expressed in rheumatoid synovia is human origin and the lymphocytic reaction to the HSP may play an important role in the pathogenesis of RA.]. 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:8823989;
    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:NP315017.RA7RoxvQmN_yEQP00cP66SN1pwSfElUCDMlShP2G3LAzg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:00+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" .
}