@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90> .
@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:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_head {
  this: np:hasAssertion dgn-np:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_assertion;
    np:hasProvenance dgn-np:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_provenance;
    np:hasPublicationInfo dgn-np:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_assertion a np:Assertion .
  
  dgn-np:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_provenance a np:Provenance .
  
  dgn-np:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_assertion {
  miriam-gene:3126 a ncit:C16612 .
  
  lld:C0019829 a ncit:C7057 .
  
  dgn-gda:DGN6e75374934a7186ec2b85fc95e90ecff sio:SIO_000628 miriam-gene:3126, lld:C0019829;
    a sio:SIO_001121 .
}

dgn-np:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_provenance {
  dgn-np:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_assertion dcterms:description
      "[To determine whether this predisposition extends to familial HD, HLA class II loci (DRB1, DQA1, DQB1, DRB3, DRB4, and DRB5) and transporter associated with antigen processing (TAP) loci (TAP1, TAP2) were investigated in 100 members of 16 families with at least 2 confirmed cases of HD.]. 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:11781255;
    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:NP889213.RADtv0d0suYFXmqp4jrc3m6976hhdz4aMJhGZG_fVIx90130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:06+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" .
}