@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw> .
@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:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_head {
  this: np:hasAssertion dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion;
    np:hasProvenance dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance;
    np:hasPublicationInfo dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion a np:Assertion .
  
  dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance a np:Provenance .
  
  dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion {
  miriam-gene:3126 a ncit:C16612 .
  
  lld:C0015773 a ncit:C7057 .
  
  dgn-gda:DGNb63840073cb08499bc1194bb3804e891 sio:SIO_000628 miriam-gene:3126, lld:C0015773;
    a sio:SIO_001121 .
}

dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_provenance {
  dgn-np:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_assertion dcterms:description
      "[Of the 83 patients, 61 (73%) possessed the DR4 allele and within this group we have investigated the relative frequencies of two DQ beta gene variants of DQw3, DQw7 and DQw8, one of which we had previously found to be raised in Felty's syndrome.]. 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:2571385;
    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:NP718937.RAdpYt8JiRTFjEEkCNvE0bevWBFaR8Ne1_WM2SplDNjTw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:16+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" .
}