@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_head {
  this: np:hasAssertion dgn-np:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_assertion;
    np:hasProvenance dgn-np:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_provenance;
    np:hasPublicationInfo dgn-np:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_assertion a np:Assertion .
  
  dgn-np:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_provenance a np:Provenance .
  
  dgn-np:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C0398623 a ncit:C7057 .
  
  dgn-gda:DGN09d5acf31df8858e23728b7c15ccb181 sio:SIO_000628 miriam-gene:2153, lld:C0398623;
    a sio:SIO_001121 .
}

dgn-np:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_provenance {
  dgn-np:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_assertion dcterms:description
      "[In our experience the prevalence of FVL and the FII G20210Amutations was significantly higher in women with unexplained stillbirth, instead the prevalence of genetic thrombophilia was high but not statistically significant in women with recurrent pregnancy loss.]. 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:16014310;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP503885.RAPAmLlLNAhMdriqRbkkw3woKNvmFVjNjR6V4BRHF-wNk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:33+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}