@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA> .
@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:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_head {
  this: np:hasAssertion dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_assertion;
    np:hasProvenance dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_provenance;
    np:hasPublicationInfo dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_assertion a np:Assertion .
  
  dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_provenance a np:Provenance .
  
  dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C0021359 a ncit:C7057 .
  
  dgn-gda:DGN972b9f40238f2926f1d7c7d41904266a sio:SIO_000628 miriam-gene:2153, lld:C0021359;
    a sio:SIO_001121 .
}

dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_provenance {
  dgn-np:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_assertion dcterms:description
      "[Factor V Leiden (FVL) G1691A, methylenetetrahydrofolate reductase (MTHFR) C677T, and factor II (FII) G20210A mutations are three important causes of thrombophilia, the condition that might be related to infertility and recurrent spontaneous abortion (RSA).]. 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:16450127;
    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:NP453762.RA8bUMHEmaULjXd2oZI4WJhmRxm6maJNOpXZZgnpwp_GA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:30+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" .
}