@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg> .
@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:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_head {
  this: np:hasAssertion dgn-np:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_assertion;
    np:hasProvenance dgn-np:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_provenance;
    np:hasPublicationInfo dgn-np:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_assertion a np:Assertion .
  
  dgn-np:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_provenance a np:Provenance .
  
  dgn-np:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGNaba1d106c6627f877dcfe5f988a763fe sio:SIO_000628 miriam-gene:4846, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_provenance {
  dgn-np:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_assertion dcterms:description
      "[Therefore, this study was planned to determine (a) role of endothelium-derived nitric oxide (NO) and endothelin as coronary artery disease (CAD) risk markers and (b) intergenotypic variation of endothelial nitric oxide synthase (eNOS) Glu298Asp polymorphism in CAD.The endothelin, NO and eNOS genotypes were determined in 60 patients with documented history of CAD.]. 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:22045428;
    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:NP935435.RAGV8_iPIuYN-RXlVfp96iU7rsTK9ee4Sa4pY4WZ3qOpg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:49+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" .
}