@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM> .
@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:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_head {
  this: np:hasAssertion dgn-np:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_assertion;
    np:hasProvenance dgn-np:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_provenance;
    np:hasPublicationInfo dgn-np:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_assertion a np:Assertion .
  
  dgn-np:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_provenance a np:Provenance .
  
  dgn-np:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0079541 a ncit:C7057 .
  
  dgn-gda:DGN2563aabb49457ed2ab60c6c9b9bfbca5 sio:SIO_000628 miriam-gene:3342, lld:C0079541;
    a sio:SIO_001121 .
}

dgn-np:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_provenance {
  dgn-np:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_assertion dcterms:description
      "[Our results may contribute to verify the effectiveness and applicability of the molecular technique of array CGH for prenatal diagnosis purposes, and contributing to the knowledge of the submicroscopic genomic instability characterization of HPE fetuses.]. 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:21359414;
    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:NP262327.RAAN0kRkTs1SxUJvaX5k6ZY22W0rVybwZr0F5vnYp72VM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}