@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs> .
@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:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_head {
  this: np:hasAssertion dgn-np:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_assertion;
    np:hasProvenance dgn-np:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_provenance;
    np:hasPublicationInfo dgn-np:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_assertion a np:Assertion .
  
  dgn-np:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_provenance a np:Provenance .
  
  dgn-np:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_assertion {
  miriam-gene:8718 a ncit:C16612 .
  
  lld:C0086445 a ncit:C7057 .
  
  dgn-gda:DGN4570516f8093f526d9061cf3aadb6838 sio:SIO_000628 miriam-gene:8718, lld:C0086445;
    a sio:SIO_001121 .
}

dgn-np:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_provenance {
  dgn-np:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_assertion dcterms:description
      "[To clarify whether C4A deletion is an independent risk factor for IMN or is increased secondarily to the Caucasoid HLA A1, B8, DR3 extended haplotype, we examined the frequency of C4A deletion in Japanese patients, in whom the disease is associated with another HLA haplotype (DR2-DQw1).]. 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:1360552;
    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:NP375276.RAqFF_s4kyPuJ2IMcUtOhCIE3-d9tkP9tG7m27bbwWXhs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:39+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" .
}