@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E> .
@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:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_head {
  this: np:hasAssertion dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_assertion ;
    np:hasProvenance dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_provenance ;
    np:hasPublicationInfo dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_assertion a np:Assertion .
  dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_provenance a np:Provenance .
  dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_assertion {
  miriam-gene:5327 a ncit:C16612 .
  lld:C0007222 a ncit:C7057 .
  dgn-gda:DGN7ea52238f9fd05480711ea207506e683 sio:SIO_000628 miriam-gene:5327 , lld:C0007222 ;
    a sio:SIO_001121 .
}
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_provenance {
  dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_assertion dcterms:description "[The observed allele frequencies of the polymorphisms of t-PA, fibrinogen, FVII, ACE, angiotensinogen and the plasma levels of PAI-1 and D-Dimer were in accordance with the low CVD risk in the Inuit, considering the observed associations between these measures and CVD risk in Caucasian populations, but for other measures this was not the case (allele frequencies of the PAI-1 polymorphism, and plasma levels of fibrinogen, FVII and t-PA).]. 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:10235437 ;
    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:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:19+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" .
}