@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc> .
@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:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_head {
  this: np:hasAssertion dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_assertion ;
    np:hasProvenance dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_provenance ;
    np:hasPublicationInfo dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_assertion a np:Assertion .
  dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_provenance a np:Provenance .
  dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_assertion {
  miriam-gene:4695 a ncit:C16612 .
  lld:C0155626 a ncit:C7057 .
  dgn-gda:DGN12defa2731cdab7f6c857564b34acdbd sio:SIO_000628 miriam-gene:4695 , lld:C0155626 ;
    a sio:SIO_001121 .
}
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_provenance {
  dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_assertion dcterms:description "[The frequencies of T allele and T/T homozygotes in patients with AMI were significantly higher than in controls and in patients with angina without prior AMI, suggesting that the CD14 promoter polymorphism is associated with AMI rather than with coronary atherosclerosis, and this polymorphism may be one of the genetic risk factors for AMI in Japanese men.]. 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:10980225 ;
    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:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:30+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" .
}