@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY> .
@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:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_head {
  this: np:hasAssertion dgn-np:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_assertion ;
    np:hasProvenance dgn-np:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_provenance ;
    np:hasPublicationInfo dgn-np:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_assertion a np:Assertion .
  dgn-np:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_provenance a np:Provenance .
  dgn-np:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_assertion {
  miriam-gene:2243 a ncit:C16612 .
  lld:C1861172 a ncit:C7057 .
  dgn-gda:DGN2c92faa177403b379fca0b13165f9172 sio:SIO_000628 miriam-gene:2243 , lld:C1861172 ;
    a sio:SIO_001122 .
}
dgn-np:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_provenance {
  dgn-np:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_assertion dcterms:description "[Data indicated that functional genetic variants in FGA are risk factors for venous thromboembolism in Taiwanese populations, and determination of FGA genotypes will likely contribute to primary prevention of this condition.]. 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:16362348 ;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP214688.RAvFRQPB2mqzNTVBg_pHOReEAyCiOUHfOzN8HaL-z5AYY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:24+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" .
}