@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_head {
  this: np:hasAssertion dgn-np:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_assertion;
    np:hasProvenance dgn-np:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_provenance;
    np:hasPublicationInfo dgn-np:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_assertion a np:Assertion .
  
  dgn-np:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_provenance a np:Provenance .
  
  dgn-np:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_assertion {
  miriam-gene:4843 a ncit:C16612 .
  
  lld:C0004153 a ncit:C7057 .
  
  dgn-gda:DGNcd7aaae31a29343fa154eb4b81e4fdfc sio:SIO_000628 miriam-gene:4843, lld:C0004153;
    a sio:SIO_001121 .
}

dgn-np:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_provenance {
  dgn-np:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_assertion dcterms:description
      "[We amplified these (AAAT) repeat variants from the NOS2A gene (denoted iNOS R4 and iNOS R5) from 325 Finnish men included in the Helsinki Sudden Death Study, and studied their association with indices of stenosis and atherosclerosis of the left anterior descending artery (LAD), right coronary artery (RCA) and left circumflex artery (LCX).]. 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:14636285;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP421897.RALsoclrPZDV8wGOTvmLo0nbVCZBWvt5b8KNC7nE5zYVQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:56+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}