@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE> .
@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:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_head {
  this: np:hasAssertion dgn-np:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_assertion;
    np:hasProvenance dgn-np:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_provenance;
    np:hasPublicationInfo dgn-np:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_assertion a np:Assertion .
  
  dgn-np:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_provenance a np:Provenance .
  
  dgn-np:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_assertion {
  miriam-gene:2626 a ncit:C16612 .
  
  lld:C0152021 a ncit:C7057 .
  
  dgn-gda:DGN67bf5301a94faac71dde10e640721061 sio:SIO_000628 miriam-gene:2626, lld:C0152021;
    a sio:SIO_001121 .
}

dgn-np:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_provenance {
  dgn-np:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_assertion dcterms:description
      "[These results suggest that genomic GATA4 and TFAP2B missense mutations may be associated with nonfamilial congenital heart disease with diverse clinical phenotypes in patients with congenital heart disease from southern China.]. 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:22959235;
    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:NP419541.RAdAmrhQq4MlWcniTQwYoHGTORfOvorS1pSEOI7JLg8aE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:44+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" .
}