@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0> .
@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:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_head {
  this: np:hasAssertion dgn-np:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_assertion;
    np:hasProvenance dgn-np:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_provenance;
    np:hasPublicationInfo dgn-np:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_assertion a np:Assertion .
  
  dgn-np:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_provenance a np:Provenance .
  
  dgn-np:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_assertion {
  miriam-gene:24 a ncit:C16612 .
  
  lld:C0040560 a ncit:C7057 .
  
  dgn-gda:DGNaf2374ffaf82e53b77f907f50119ff0c sio:SIO_000628 miriam-gene:24, lld:C0040560;
    a sio:SIO_001122 .
}

dgn-np:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_provenance {
  dgn-np:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_assertion dcterms:description
      "[These associations between clinical outcomes of congenital toxoplasmosis and polymorphisms at ABCA4 and COL2A1 provide novel insight into the molecular pathways that can be affected by congenital infection with this parasite.]. 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:18523590;
    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:NP75462.RA3NUEEqy167-T8F0L4omAhXFT_0h2mpAAXrmJu2Js2m0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:36+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" .
}