@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg> .
@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:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_head {
  this: np:hasAssertion dgn-np:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_assertion;
    np:hasProvenance dgn-np:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_provenance;
    np:hasPublicationInfo dgn-np:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_assertion a np:Assertion .
  
  dgn-np:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_provenance a np:Provenance .
  
  dgn-np:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_assertion {
  miriam-gene:2268 a ncit:C16612 .
  
  lld:C0005779 a ncit:C7057 .
  
  dgn-gda:DGNf13db6ae33c8e6bbb7e8fa5f0e390287 sio:SIO_000628 miriam-gene:2268, lld:C0005779;
    a sio:SIO_001121 .
}

dgn-np:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_provenance {
  dgn-np:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_assertion dcterms:description
      "[To determine to what extent double inherited thrombophilias are associated with adverse obstetric complications correlated with fetoplacental insufficiency, such as preeclampsia, hemolytic anemia elevated liver enzymes and low platelet count (HELLP) syndrome, gestational hypertension, fetal growth restriction (FGR), intrauterine death (ID), abruptio placentae and disseminated intravascular coagulopathy.]. 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:20868443;
    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:NP308397.RA65lTr9bbUhnUn1SwRatRc_GKm5btFzFYqFa3YA1tQJg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:57+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" .
}