@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88> .
@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:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_head {
  this: np:hasAssertion dgn-np:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_assertion;
    np:hasProvenance dgn-np:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_provenance;
    np:hasPublicationInfo dgn-np:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_assertion a np:Assertion .
  
  dgn-np:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_provenance a np:Provenance .
  
  dgn-np:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C1135868 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_provenance {
  dgn-np:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_assertion dcterms:description
      "[The purpose of this study was to determine whether HCG beta gene deletions occur in women with recurrent abortion or primary unexplained infertility, and whether HCG beta gene duplications are present in women with GTN.]. 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:9237259;
    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:NP696053.RAFG0RXWCIRMUS3bZPywI42Uk2sz0_bR4qh9Pzb469O88130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:03+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}