@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU> .
@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:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_head {
  this: np:hasAssertion dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_assertion;
    np:hasProvenance dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_provenance;
    np:hasPublicationInfo dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_assertion a np:Assertion .
  
  dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_provenance a np:Provenance .
  
  dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_assertion {
  miriam-gene:3127 a ncit:C16612 .
  
  lld:C0032026 a ncit:C7057 .
  
  dgn-gda:DGN05c56015a58a05f2f83709573284c59b sio:SIO_000628 miriam-gene:3127, lld:C0032026;
    a sio:SIO_001122 .
}

dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_provenance {
  dgn-np:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_assertion dcterms:description
      "[We suggest that alleles DQB1*04 may be involved in the genetic susceptibility of PR based on the significant predominance of those alleles observed in the black PR patients. We also recommend that more studies are conducted on populations of other ethnic origins, preferentially with higher resolution techniques of DNA typing.]. 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:16405603;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP67083.RAsUO5W0Y8k4MB78sV2G-PV3E9XzxdM-DYd_SM-sQt6ZU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}