@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM> .
@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:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_head {
  this: np:hasAssertion dgn-np:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_assertion;
    np:hasProvenance dgn-np:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_provenance;
    np:hasPublicationInfo dgn-np:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_assertion a np:Assertion .
  
  dgn-np:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_provenance a np:Provenance .
  
  dgn-np:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_assertion {
  miriam-gene:1368 a ncit:C16612 .
  
  lld:C0152164 a ncit:C7057 .
  
  dgn-gda:DGNd570fa833711f27ef34c10cdb45e6546 sio:SIO_000628 miriam-gene:1368, lld:C0152164;
    a sio:SIO_001121 .
}

dgn-np:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_provenance {
  dgn-np:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_assertion dcterms:description
      "[About 2 per cent of specimens from chorionic villus sampling (CVS) analysed either on direct preparation of cytotrophoblast cells or after culture of mesenchymal stroma reveal confined placental mosaicism (CPM), most commonly involving chromosomal trisomy.]. 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:1800987;
    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:NP264686.RA3zps3ViJQYdtvi7i6GBj8FU7QN_wnRYxIW2YZFNJmdM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}