@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s> .
@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/v4.0.0/void/> .

dgn-np:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_head {
  this: np:hasAssertion dgn-np:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_assertion;
    np:hasProvenance dgn-np:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_provenance;
    np:hasPublicationInfo dgn-np:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_assertion a np:Assertion .
  
  dgn-np:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_provenance a np:Provenance .
  
  dgn-np:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_assertion {
  miriam-gene:2626 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN04d91cacd43962708c76b83f96537df8 sio:SIO_000628 miriam-gene:2626, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_provenance {
  dgn-np:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_assertion dcterms:description
      "[Consistent with previous findings, GATA4 mutations that result in deficits in transactivation ability are consistently associated with CHD suggesting that normal transactivation properties of GATA4 are required for proper cardiac development.]. 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:17352393;
    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:NP598430.RASvpaMVDkEDozRdrsI5RoRJBWGHpr3xI13CQlew9P6-s130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:17+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" .
}