@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I> .
@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:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_head {
  this: np:hasAssertion dgn-np:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_assertion;
    np:hasProvenance dgn-np:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_provenance;
    np:hasPublicationInfo dgn-np:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_assertion a np:Assertion .
  
  dgn-np:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_provenance a np:Provenance .
  
  dgn-np:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_assertion {
  miriam-gene:3126 a ncit:C16612 .
  
  lld:C0030807 a ncit:C7057 .
  
  dgn-gda:DGNb3b1f042359b3aee73b38bb4020e8134 sio:SIO_000628 miriam-gene:3126, lld:C0030807;
    a sio:SIO_001121 .
}

dgn-np:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_provenance {
  dgn-np:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_assertion dcterms:description
      "[The observation that both diseases, pemphigus vulgaris and pemphigus foliaceus, carry the same susceptible human leukocyte antigen alleles has been interpreted as a common genetic background predisposing to pemphigus as, like in other autoimmune disorders, it is not sufficient to explain the onset of the disease on the basis of the sole aforementioned alleles.]. 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:10417627;
    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:NP318353.RA5H4t4SPWpdI-HGoy4l9AlXXvjLVWe4oiOdsS9PaTM1I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:04+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" .
}