@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs> .
@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:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_head {
  this: np:hasAssertion dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion;
    np:hasProvenance dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance;
    np:hasPublicationInfo dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion a np:Assertion .
  
  dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance a np:Provenance .
  
  dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion {
  miriam-gene:3670 a ncit:C16612 .
  
  lld:C0018818 a ncit:C7057 .
  
  dgn-gda:DGN0af597c3ebeac403027a65767f5dc1c3 sio:SIO_000628 miriam-gene:3670, lld:C0018818;
    a sio:SIO_001121 .
}

dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance {
  dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion dcterms:description
      "[ISL1 is related to the atrial septal defect group and the ventricular septal defect group, and the genotypes were associated with the occurrence of CHD in the dominant mode of inheritance.]. 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:24634231;
    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:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:45+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" .
}