@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE> .
@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:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_head {
  this: np:hasAssertion dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_assertion;
    np:hasProvenance dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_provenance;
    np:hasPublicationInfo dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_assertion a np:Assertion .
  
  dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_provenance a np:Provenance .
  
  dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C0085083 a ncit:C7057 .
  
  dgn-gda:DGNc2cb77c2935c92196e826e0449969a76 sio:SIO_000628 miriam-gene:2153, lld:C0085083;
    a sio:SIO_001121 .
}

dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_provenance {
  dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_assertion dcterms:description
      "[The results of this study suggest that FVL and PGM presence in asymptomatic women and in the absence of other risk factors do not influence IVF outcome, or represent risk factors for ovarian hyperstimulation syndrome (OHSS), or favour thrombosis after IVF.]. 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:21868400;
    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:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:03+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" .
}