@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_head {
  this: np:hasAssertion dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_assertion;
    np:hasProvenance dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_provenance;
    np:hasPublicationInfo dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_assertion a np:Assertion .
  
  dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_provenance a np:Provenance .
  
  dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_assertion {
  miriam-gene:2492 a ncit:C16612 .
  
  lld:C0085083 a ncit:C7057 .
  
  dgn-gda:DGNf43b634ca5351351dca2ccb85d21f317 sio:SIO_000628 miriam-gene:2492, lld:C0085083;
    a sio:SIO_001121 .
}

dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_provenance {
  dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_assertion dcterms:description
      "[The paper focuses on the recent identification of mutations in the FSH receptor gene that display an increased sensitivity to hCG and are responsible for the development of spontaneous OHSS occurring during pregnancy.]. 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:16034183;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:34+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}