@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8> .
@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:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_head {
  this: np:hasAssertion dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_assertion;
    np:hasProvenance dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_provenance;
    np:hasPublicationInfo dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_assertion a np:Assertion .
  
  dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_provenance a np:Provenance .
  
  dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_assertion {
  miriam-gene:2626 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN58d6facee00d776ddeeb0e95c6d471f3 sio:SIO_000628 miriam-gene:2626, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_provenance {
  dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_assertion dcterms:description
      "[We confirmed the contribution to CHD of copy number changes in genes such as GATA4 and NODAL and identified several genes in novel recurrent CNVs that may point to novel CHD candidate loci.]. 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:23979609;
    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:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:07+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" .
}