@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4> .
@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:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_head {
  this: np:hasAssertion dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_assertion ;
    np:hasProvenance dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_provenance ;
    np:hasPublicationInfo dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_assertion a np:Assertion .
  dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_provenance a np:Provenance .
  dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_assertion {
  miriam-gene:342977 a ncit:C16612 .
  lld:C0027051 a ncit:C7057 .
  dgn-gda:DGN13058795866211deb9f2ddd40ab3f6ca sio:SIO_000628 miriam-gene:342977 , lld:C0027051 ;
    a sio:SIO_001121 .
}
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_provenance {
  dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_assertion dcterms:description "[We studied two polymorphisms of the NOS3 gene, the VNTR in intron 4 (4VNTR) and the Glu298Asp polymorphism in exon 7, in relation to the existence of premature coronary artery disease and the occurrence of myocardial infarction.A total number of 370 individuals of the Greek population was examined by PCR-RFLP method.The patient group consisted of 209 subjects, aged less than 58 years presenting symptomatic coronary artery disease, documented by coronary angiography.]. 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:19014005 ;
    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:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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" .
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}