@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY> .
@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:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_head {
  this: np:hasAssertion dgn-np:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_assertion;
    np:hasProvenance dgn-np:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_provenance;
    np:hasPublicationInfo dgn-np:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_assertion a np:Assertion .
  
  dgn-np:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_provenance a np:Provenance .
  
  dgn-np:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_assertion {
  miriam-gene:7290 a ncit:C16612 .
  
  lld:C0039685 a ncit:C7057 .
  
  dgn-gda:DGN673640f59e06dca7cda0447740171469 sio:SIO_000628 miriam-gene:7290, lld:C0039685;
    a sio:SIO_001121 .
}

dgn-np:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_provenance {
  dgn-np:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_assertion dcterms:description
      "[Eighty-four children with sporadic tetralogy of Fallot (40 boys and 44 girls; mean age, 34 months) were analyzed for microdeletion at chromosome 22q11 by genotype analysis, using five microsatellite markers, D22S427, D22S941, D22S944, D22S264 and D22S311, and confirmed by quantitative polymerase chain reaction, using TUPLE1 and D22S264.]. 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:10390265;
    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:NP260271.RAUDlywLvap9ZLCDAqrAFMJWIoK-KdyPlQ_txvXlHvKFY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:25+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" .
}