@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ> .
@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:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_head {
  this: np:hasAssertion dgn-np:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_assertion;
    np:hasProvenance dgn-np:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_provenance;
    np:hasPublicationInfo dgn-np:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_assertion a np:Assertion .
  
  dgn-np:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_provenance a np:Provenance .
  
  dgn-np:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_assertion {
  miriam-gene:7168 a ncit:C16612 .
  
  lld:C1292769 a ncit:C7057 .
  
  dgn-gda:DGN9bae9bd3a57dcd6209005959b8d0a511 sio:SIO_000628 miriam-gene:7168, lld:C1292769;
    a sio:SIO_001121 .
}

dgn-np:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_provenance {
  dgn-np:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_assertion dcterms:description
      "[The present study was conducted to investigate the association of N-terminal pro-B-type natriuretic peptide (NT-pro-BNP) levels with LV remodeling on magnetic resonance imaging and procollagen formation in 17 healthy controls and 24 patients with nonobstructive HC attributable to an identical Asp175Asn (aspartic acid to asparagine at codon 175) mutation in the alpha-tropomyosin gene.]. 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:18394456;
    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:NP520453.RAuOLbM_tjofm2aEIQ0D7cxF7WIGNJ_XzNFAix3FdwpMQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:10+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" .
}