@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8> .
@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:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_head {
  this: np:hasAssertion dgn-np:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_assertion;
    np:hasProvenance dgn-np:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_provenance;
    np:hasPublicationInfo dgn-np:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_assertion a np:Assertion .
  
  dgn-np:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_provenance a np:Provenance .
  
  dgn-np:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0155626 a ncit:C7057 .
  
  dgn-gda:DGNa7463fd32650dc12eb35fc422a16e154 sio:SIO_000628 miriam-gene:4846, lld:C0155626;
    a sio:SIO_001121 .
}

dgn-np:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_provenance {
  dgn-np:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_assertion dcterms:description
      "[Given the role of nitric oxide in the vascular system, we aimed to test hypotheses of synergy between the common endothelial nitric oxide synthase (eNOS) Asp298 allele and T2DM in predisposing to acute myocardial infarction (AMI).]. 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:19077211;
    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:NP368600.RAaHpBZupQC_cublzmLmLG6b4mLMhdSfVluPTlwBpKRM8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:35+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" .
}