@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A> .
@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:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_head {
  this: np:hasAssertion dgn-np:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion;
    np:hasProvenance dgn-np:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_provenance;
    np:hasPublicationInfo dgn-np:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion a np:Assertion .
  
  dgn-np:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_provenance a np:Provenance .
  
  dgn-np:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion {
  miriam-gene:29123 a ncit:C16612 .
  
  lld:C3714756 a ncit:C7057 .
  
  dgn-gda:DGNc66382d7f2f59c42e312c2780344f537 sio:SIO_000628 miriam-gene:29123, lld:C3714756;
    a sio:SIO_001121 .
}

dgn-np:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_provenance {
  dgn-np:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion dcterms:description
      "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. 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:23335808;
    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:NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:45+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" .
}