@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I> .
@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:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_head {
  this: np:hasAssertion dgn-np:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_assertion;
    np:hasProvenance dgn-np:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_provenance;
    np:hasPublicationInfo dgn-np:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_assertion a np:Assertion .
  
  dgn-np:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_provenance a np:Provenance .
  
  dgn-np:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_assertion {
  miriam-gene:3123 a ncit:C16612 .
  
  lld:C0007570 a ncit:C7057 .
  
  dgn-gda:DGNf63c597352310f15bedc626d97e18bfb sio:SIO_000628 miriam-gene:3123, lld:C0007570;
    a sio:SIO_001121 .
}

dgn-np:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_provenance {
  dgn-np:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_assertion dcterms:description
      "[To study the possible influence of DRB1 or other DQA1 and DQB1 alleles on the CD susceptibility conferred by these DQ genes, we performed genomic HLA typing of 94 CD patients, selected those who carried at least one copy of the DRB1*0301-DQA1*0501-DQB1*0201 haplotype (N = 89) and compared them to 47 random, healthy Norwegians matched with the patients to carry at least one copy of the above haplotype.]. 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:8362409;
    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:NP306621.RAiI-HXF9O2Lf1_KRy5Rab4kf1E_Psf_ai6KpwsVV7M9I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:56+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" .
}