@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc> .
@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/v3.0.0/void/> .

dgn-np:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_head {
  this: np:hasAssertion dgn-np:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_assertion;
    np:hasProvenance dgn-np:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_provenance;
    np:hasPublicationInfo dgn-np:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_assertion a np:Assertion .
  
  dgn-np:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_provenance a np:Provenance .
  
  dgn-np:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_assertion {
  miriam-gene:308 a ncit:C16612 .
  
  lld:C0398623 a ncit:C7057 .
  
  dgn-gda:DGN99cae0fb0a27779040fc46552610c511 sio:SIO_000628 miriam-gene:308, lld:C0398623;
    a sio:SIO_001121 .
}

dgn-np:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_provenance {
  dgn-np:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_assertion dcterms:description
      "[Although preliminary, these results suggest that hypomorphic M2 alleles in the in placental ANXA5 promoter, whether transmitted maternally or paternally, might be an essential determinant of an increased risk of pre-eclampsia via local thrombophilia at the feto-maternal interface.]. 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:24140079;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP239881.RAdVScUwWPfGBX7QLP_S5MZ8YPjQEz9_hgD64hdp6lyNc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:56+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}