@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw> .
@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:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_head {
  this: np:hasAssertion dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_assertion ;
    np:hasProvenance dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_provenance ;
    np:hasPublicationInfo dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_assertion a np:Assertion .
  dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_provenance a np:Provenance .
  dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_assertion {
  miriam-gene:4552 a ncit:C16612 .
  lld:C1861172 a ncit:C7057 .
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}
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_provenance {
  dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_assertion dcterms:description "[ Prothrombin and factor V polymorphisms increased the risk for VTE in women, independent from other established risk factors. Although hyperhomocysteinaemia also heightens this risk, common polymorphisms in two genes that are responsible for homocysteine remethylation do not. These findings are consistent with previous studies that included both men and women.]. 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:11806787 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
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}