@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU> .
@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:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_head {
  this: np:hasAssertion dgn-np:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_assertion ;
    np:hasProvenance dgn-np:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_provenance ;
    np:hasPublicationInfo dgn-np:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_assertion a np:Assertion .
  dgn-np:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_provenance a np:Provenance .
  dgn-np:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_assertion {
  miriam-gene:2157 a ncit:C16612 .
  lld:C0015503 a ncit:C7057 .
  dgn-gda:DGN79075924037ee3b1cf189785406a9b0a sio:SIO_000628 miriam-gene:2157 , lld:C0015503 ;
    a sio:SIO_001122 .
}
dgn-np:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_provenance {
  dgn-np:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_assertion dcterms:description "[ These results highlight the importance of a concerted effect of multiple genetic factors in determining FVII levels. Since there is evidence that FVII levels constitute a risk factor for coronary heart disease and considering the importance of F7 DNA polymorphisms in determining FVII levels, further analyses of these polymorphisms should yield information to aid the understanding of the quantitative variation in FVII levels and the relative genetic risk for cardiovascular disease in the general population.]. 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:12935978 ;
    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:NP44325.RAbi8y0uq_tItahlPtmBQLsy9wuXlnPvWvWkO0MpHxgmU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
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}