@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g> .
@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:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_head {
  this: np:hasAssertion dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_assertion;
    np:hasProvenance dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_provenance;
    np:hasPublicationInfo dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_assertion a np:Assertion .
  
  dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_provenance a np:Provenance .
  
  dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_assertion {
  miriam-gene:5242 a ncit:C16612 .
  
  lld:C0000786 a ncit:C7057 .
  
  dgn-gda:DGN4074b10c9a9e436280cd5c847a45a7e1 sio:SIO_000628 miriam-gene:5242, lld:C0000786;
    a sio:SIO_001121 .
}

dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_provenance {
  dgn-np:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_assertion dcterms:description
      "[To compare the incidence of chromosomal abnormalities in preimplantation embryos from couples undergoing preimplantation genetic screening (PGS) after previous aneuploid miscarriage after either natural conception (NC) or assisted reproductive technology (ART) versus fertile couples who underwent PGS for sex-linked diseases as a control group.]. 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:22521156;
    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:NP683508.RA1AtsgbTgSPNMPJVXzVCwxbtoP0WhOXAMFWOQtLu7W4g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}