@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ> .
@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:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_head {
  this: np:hasAssertion dgn-np:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion;
    np:hasProvenance dgn-np:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_provenance;
    np:hasPublicationInfo dgn-np:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion a np:Assertion .
  
  dgn-np:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_provenance a np:Provenance .
  
  dgn-np:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGN158502f51697120dee414a5628578388 sio:SIO_000628 miriam-gene:3342, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_provenance {
  dgn-np:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_assertion dcterms:description
      "[In severe ID, cytogenetically visible chromosomal abnormalities like trisomy 21 continue to be common, but since the introduction of array CGH, it is becoming clear that submicroscopic deletions and duplications are equally frequent, yet previously overlooked causes of ID.]. 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:18694825;
    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:NP893161.RAaH8HVrprIIVN1CdnObNsz2raVTJOUj7rPYDe5hs97IQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:09+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" .
}