@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg> .
@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:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_head {
  this: np:hasAssertion dgn-np:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_assertion;
    np:hasProvenance dgn-np:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_provenance;
    np:hasPublicationInfo dgn-np:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_assertion a np:Assertion .
  
  dgn-np:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_provenance a np:Provenance .
  
  dgn-np:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0398623 a ncit:C7057 .
  
  dgn-gda:DGN4bc9f5b48b2154e7799e810466c779f4 sio:SIO_000628 miriam-gene:4524, lld:C0398623;
    a sio:SIO_001122 .
}

dgn-np:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_provenance {
  dgn-np:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_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-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:NP533870.RArJ7HKiueNrbbjB0r2nnH1Ep_zm2eFscuDq4y4v-ErKg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:46+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" .
}