@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ> .
@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:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_head {
  this: np:hasAssertion dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_assertion;
    np:hasProvenance dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_provenance;
    np:hasPublicationInfo dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_assertion a np:Assertion .
  
  dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_provenance a np:Provenance .
  
  dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_assertion {
  miriam-gene:1861 a ncit:C16612 .
  
  lld:C0018213 a ncit:C7057 .
  
  dgn-gda:DGN1c768068276c7ecb0ff6e80fb6d059a1 sio:SIO_000628 miriam-gene:1861, lld:C0018213;
    a sio:SIO_001121 .
}

dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_provenance {
  dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_assertion dcterms:description
      "[Furthermore the transmission analysis in GD and HT families revealed no differences in alleles transmission for rs1990760 IFIH1 from parents with or without HLA risk haplotype DQ2 to the affected offspring.]. 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:19961590;
    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:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:09+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" .
}