@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs> .
@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:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_head {
   this: np:hasAssertion dgn-np:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_assertion ;
    np:hasProvenance dgn-np:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_provenance ;
    np:hasPublicationInfo dgn-np:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_assertion a np:Assertion .
  dgn-np:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_provenance a np:Provenance .
  dgn-np:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_assertion {
   miriam-gene:118 a ncit:C16612 .
  lld:C0085096 a ncit:C7057 .
  dgn-gda:DGN17bdd6c32fe1ee13b41ae2e43708880c sio:SIO_000628 miriam-gene:118 , lld:C0085096 ;
    a sio:SIO_001122 .
}
dgn-np:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_provenance {
   dgn-np:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_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:NP76993.RAAEjNmQvH6uParbWLnKYYR0Q0MTlPpQoI1h6FLQ1hhbs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:37+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" .
}