@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs> .
@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/v3.0.0/void/> .

dgn-np:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_head {
  this: np:hasAssertion dgn-np:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_assertion;
    np:hasProvenance dgn-np:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_provenance;
    np:hasPublicationInfo dgn-np:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_assertion a np:Assertion .
  
  dgn-np:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_provenance a np:Provenance .
  
  dgn-np:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_assertion {
  miriam-gene:126393 a ncit:C16612 .
  
  lld:C0007193 a ncit:C7057 .
  
  dgn-gda:DGNe50e7e17091ef7ca5582f89a4e13f87b sio:SIO_000628 miriam-gene:126393, lld:C0007193;
    a sio:SIO_001121 .
}

dgn-np:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_provenance {
  dgn-np:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_assertion dcterms:description
      "[To determine whether genetic variants exist in human Hsp20, which may modify these beneficial effects, we sequenced the coding region of the Hsp20 gene in 1347 patients suffering from dilated cardiomyopathy and 744 subjects with no heart disease.]. 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:18790732;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP968575.RAvnx0FjLO7XqWeWbJ4juX8mq17VSIWHsVXThnXfqBUzs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:31+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}