@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk> .
@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:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_head {
   this: np:hasAssertion dgn-np:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_assertion ;
    np:hasProvenance dgn-np:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_provenance ;
    np:hasPublicationInfo dgn-np:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_assertion a np:Assertion .
  dgn-np:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_provenance a np:Provenance .
  dgn-np:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_assertion {
   miriam-gene:4547 a ncit:C16612 .
  lld:C0085096 a ncit:C7057 .
  dgn-gda:DGN46647f5a0164e4c238830715afa1ff4c sio:SIO_000628 miriam-gene:4547 , lld:C0085096 ;
    a sio:SIO_001122 .
}
dgn-np:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_provenance {
   dgn-np:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_assertion dcterms:description "[Twenty-three polymorphisms in 22 potential PAD candidate genes (F2, FGB, MTHFR, ITGB3, ACE, AGT, IL6, CCL2, ICAM1, SELE, MMP9, PPARG, MMP1, ADD1, P2RY12, LIPC, PLA2G7, SCARB1, MMP3, MTTP, LPA, CHRNA3) showed a significant association in individual studies.]. 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:19435865 ;
    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:NP69348.RAVTm2ETwOYPcFiJFyOsxFNJXT9rFFQa3KZgw7Z_30Ovk130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:33+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" .
}