@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg> .
@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:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_head {
  this: np:hasAssertion dgn-np:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_assertion ;
    np:hasProvenance dgn-np:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_provenance ;
    np:hasPublicationInfo dgn-np:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_assertion a np:Assertion .
  dgn-np:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_provenance a np:Provenance .
  dgn-np:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_assertion {
  miriam-gene:241 a ncit:C16612 .
  lld:C0010054 a ncit:C7057 .
  dgn-gda:DGNed16e4b29c4a0e6ec0071a8d0410d8ea sio:SIO_000628 miriam-gene:241 , lld:C0010054 ;
    a sio:SIO_001121 .
}
dgn-np:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_provenance {
  dgn-np:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_assertion dcterms:description "[We also review in more detail studies that have revealed an association of ischemic stroke with polymorphisms of proinflammatory genes of particular interest (LTA, IL6, and ALOX5AP) as well as with polymorphisms at chromosomal region 9p21.3, which has recently been identified as a susceptibility locus for coronary heart disease.]. 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:19075735 ;
    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:NP722995.RAhqNV2JndcqDG2UrdmAw6LJm5RTzYxBNVh36hooHfxCg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:19+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" .
}