@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio> .
@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:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_head {
  this: np:hasAssertion dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_assertion;
    np:hasProvenance dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_provenance;
    np:hasPublicationInfo dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_assertion a np:Assertion .
  
  dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_provenance a np:Provenance .
  
  dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0010073 a ncit:C7057 .
  
  dgn-gda:DGNa04351ad4779dadf508ca5ba7e1eb386 sio:SIO_000628 miriam-gene:4846, lld:C0010073;
    a sio:SIO_001121 .
}

dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_provenance {
  dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_assertion dcterms:description
      "[Multiple logistic regression analysis with forward stepwise selection using the environmental risk factors and the eNOS gene variant revealed that the most predictive independent risk factor for coronary spasm was the mutant allele (P<0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:10359729;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:09+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" .
}