@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY> .
@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:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_head {
  this: np:hasAssertion dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_assertion;
    np:hasProvenance dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_provenance;
    np:hasPublicationInfo dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_assertion a np:Assertion .
  
  dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_provenance a np:Provenance .
  
  dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_assertion {
  miriam-gene:29974 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN623eae6497d0396082d325a7d88965b5 sio:SIO_000628 miriam-gene:29974, lld:C0003873;
    a sio:SIO_001121 .
}

dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_provenance {
  dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_assertion dcterms:description
      "[DNA from the French Caucasian population was available for two samples of 100 families with one RA patient and both parents, and for 88 RA index cases from RA ASP families.]. 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:16277672;
    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:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:29+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" .
}