@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg> .
@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:NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg130_head {
  this: np:hasAssertion dgn-np:NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg130_assertion ;
    np:hasProvenance dgn-np:NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg130_provenance ;
    np:hasPublicationInfo dgn-np:NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg130_provenance a np:Provenance .
  dgn-np:NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg130_assertion {
  miriam-gene:3383 a ncit:C16612 .
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    a sio:SIO_001121 .
}
dgn-np:NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg130_provenance {
  dgn-np:NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg130_assertion dcterms:description "[The aim of the study was to assess the association between ICAM1 rs5498 polymorphism and CAD and to establish whether there are any interactions between this polymorphism and traditional risk factors in determining the risk of CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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dgn-np:NP189941.RAbJnv8BbAg5XgvgUciZOZmB-DwmNnENxt3-E0BCB4Yeg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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}