@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw> .
@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:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_head {
  this: np:hasAssertion dgn-np:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_assertion;
    np:hasProvenance dgn-np:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_provenance;
    np:hasPublicationInfo dgn-np:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_assertion a np:Assertion .
  
  dgn-np:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_provenance a np:Provenance .
  
  dgn-np:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_assertion {
  miriam-gene:3126 a ncit:C16612 .
  
  lld:C0005411 a ncit:C7057 .
  
  dgn-gda:DGNbb6f85a5b0c72ef2a2524fe5e3878e2a sio:SIO_000628 miriam-gene:3126, lld:C0005411;
    a sio:SIO_001121 .
}

dgn-np:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_provenance {
  dgn-np:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_assertion dcterms:description
      "[This study suggests that immunogenetic factors may play a role in determining susceptibility to EHBA, and the different HLA frequencies in those with and without anomalies lend support to the hypothesis that biliary atresia may be an etiologically heterogeneous disorder.]. 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:8450374;
    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:NP761753.RAZ_IZVgMXlh-YXhx_Nw81VBxX_q52SSLfScAAaS_iPFw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:41+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" .
}