@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0> .
@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:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_head {
  this: np:hasAssertion dgn-np:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_assertion;
    np:hasProvenance dgn-np:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_provenance;
    np:hasPublicationInfo dgn-np:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_assertion a np:Assertion .
  
  dgn-np:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_provenance a np:Provenance .
  
  dgn-np:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_assertion {
  miriam-gene:342977 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGN9a86d56ab976f7440dcd763bd2b1efdb sio:SIO_000628 miriam-gene:342977, lld:C0027051;
    a sio:SIO_001121 .
}

dgn-np:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_provenance {
  dgn-np:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_assertion dcterms:description
      "[Recently, a Glu298Asp variant of the endothelial nitric oxide synthase gene (NOS3) was identified as being associated with coronary spasm and myocardial infarction, whereas it has been reported that endothelial nitric oxide synthase plays a role in HP.]. 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:11745998;
    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:NP269756.RAS8iWL21cGy4NmWwXxUwcYUoLAnNkVJXOdWcP3qHn3c0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:30+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" .
}