@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM> .
@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:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_head {
  this: np:hasAssertion dgn-np:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_assertion;
    np:hasProvenance dgn-np:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_provenance;
    np:hasPublicationInfo dgn-np:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_assertion a np:Assertion .
  
  dgn-np:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_provenance a np:Provenance .
  
  dgn-np:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_assertion {
  miriam-gene:23493 a ncit:C16612 .
  
  lld:C0018816 a ncit:C7057 .
  
  dgn-gda:DGN04b25ba718780e22ca596d736596d40d sio:SIO_000628 miriam-gene:23493, lld:C0018816;
    a sio:SIO_001121 .
}

dgn-np:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_provenance {
  dgn-np:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_assertion dcterms:description
      "[By direct sequencing, we analyzed the sequences encoding the bHLH domain of the human HEY2 in 52 explanted hearts of unrelated patients with complex cardiac malformations, notably ventricular (VSD) and atrioventricular septal defects (AVSD).]. 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:16329098;
    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:NP827165.RA6p_Y63es4OYlSgNVKmwN_wKVMqemyHPgfEtFnS5aVFM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:26+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" .
}