@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM> .
@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:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_head {
  this: np:hasAssertion dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_assertion ;
    np:hasProvenance dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_provenance ;
    np:hasPublicationInfo dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_assertion a np:Assertion .
  dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_provenance a np:Provenance .
  dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_assertion {
  miriam-gene:5660 a ncit:C16612 .
  lld:C0028754 a ncit:C7057 .
  dgn-gda:DGNf0d426961579fd6d40d23c9d121bc623 sio:SIO_000628 miriam-gene:5660 , lld:C0028754 ;
    a sio:SIO_001121 .
}
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_provenance {
  dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_assertion dcterms:description "[Common genetic polymorphisms in European-Ancestry populations, such as factor V Leiden and prothrombin G20210A, and environmental risk factors, such as obesity, may account for some of the increased risk in European populations, and high factor VIII, high von Willebrand factor and low protein C levels and increased prevalence of obesity may explain some of the increased risk in African-Americans.]. 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:21797965 ;
    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:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:49+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" .
}