@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c> .
@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 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:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_head {
  this: np:hasAssertion dgn-np:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_assertion;
    np:hasProvenance dgn-np:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_provenance;
    np:hasPublicationInfo dgn-np:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_assertion a np:Assertion .
  
  dgn-np:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_provenance a np:Provenance .
  
  dgn-np:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_assertion {
  miriam-gene:1906 a ncit:C16612 .
  
  lld:C1449563 a ncit:C7057 .
  
  dgn-gda:DGNa37cafced5cda5741aa44c19968f1313 sio:SIO_000628 miriam-gene:1906, lld:C1449563;
    a sio:SIO_001121 .
}

dgn-np:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_provenance {
  dgn-np:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_assertion dcterms:description
      "[We hypothesized that genetic abnormalities of the endothelin pathway may be involved in idiopathic dilated cardiomyopathy pathophysiology and therefore examined the possible association between idiopathic dilated cardiomyopathy and polymorphisms in genes encoding endothelin 1, endothelin type A and type B receptors, in a case-control study (433 patients and 400 age- and sex-matched control subjects).]. 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:10529327;
    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:NP265785.RA_ORZKI7aP2aOoAPVRhZxYEtI8meqfEF_43Qnonvgd5c130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:46+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" .
}