@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o> .
@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:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_head {
  this: np:hasAssertion dgn-np:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_assertion;
    np:hasProvenance dgn-np:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_provenance;
    np:hasPublicationInfo dgn-np:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_assertion a np:Assertion .
  
  dgn-np:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_provenance a np:Provenance .
  
  dgn-np:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0040038 a ncit:C7057 .
  
  dgn-gda:DGNd52ddd5a3f9e0078f63d6a14d3f4a3d1 sio:SIO_000628 miriam-gene:4524, lld:C0040038;
    a sio:SIO_001122 .
}

dgn-np:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_provenance {
  dgn-np:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_assertion dcterms:description
      "[Available conclusions of pathological analysis of placentas were found to have a very high proportion of maternal vascular disease of the placenta in patients with at least one positive risk marker for thromboembolism, specially in case of association with the C677T MTHFR homozygous genotype, compared to patients with negative markers (p &lt;10(-4)).]. 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:10404763;
    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:NP257641.RAziP4LSA7oAPLnzv0iUZYWMD6pqMmSR5_V3S9Oq9gf_o130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:42+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" .
}