@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis> .
@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:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_head {
  this: np:hasAssertion dgn-np:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_assertion;
    np:hasProvenance dgn-np:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_provenance;
    np:hasPublicationInfo dgn-np:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_assertion a np:Assertion .
  
  dgn-np:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_provenance a np:Provenance .
  
  dgn-np:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0032914 a ncit:C7057 .
  
  dgn-gda:DGN461ee871abfe09cac0b0ef0939a133d9 sio:SIO_000628 miriam-gene:4524, lld:C0032914;
    a sio:SIO_001122 .
}

dgn-np:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_provenance {
  dgn-np:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_assertion dcterms:description
      "[ We didn't find any difference in the prevalence of genetic mutations in patients with preeclampsia compared to the control group. The prevalence of APC resistance was statistically higher in preeclamptic patients compared to the control group.]. 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:12879654;
    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:NP61376.RAX17cgeTBKltLWeYeIs7X_IzO2_SO3dAWGLEhocWQXis130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}