@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ> .
@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:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_head {
  this: np:hasAssertion dgn-np:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_assertion;
    np:hasProvenance dgn-np:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_provenance;
    np:hasPublicationInfo dgn-np:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_assertion a np:Assertion .
  
  dgn-np:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_provenance a np:Provenance .
  
  dgn-np:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_assertion {
  miriam-gene:6997 a ncit:C16612 .
  
  lld:C0018818 a ncit:C7057 .
  
  dgn-gda:DGN5320a15a273ea7a730e498ce04e2620b sio:SIO_000628 miriam-gene:6997, lld:C0018818;
    a sio:SIO_001121 .
}

dgn-np:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_provenance {
  dgn-np:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_assertion dcterms:description
      "[This work firstly provides human genetic evidence of TDGF1 involved in the pathogenesis of VSD, expanding our knowledge of the causative mutations of congenital heart defects, in particular, the causative mutations of VSD.]. 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:19853938;
    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:NP771433.RAVii9DZD29Y1LEQIy2Dx42VXT_f0dpCCx7BasMLFQNmQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:34+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" .
}