@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA> .
@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:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_head {
  this: np:hasAssertion dgn-np:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_assertion;
    np:hasProvenance dgn-np:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_provenance;
    np:hasPublicationInfo dgn-np:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_assertion a np:Assertion .
  
  dgn-np:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_provenance a np:Provenance .
  
  dgn-np:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_assertion {
  miriam-gene:6046 a ncit:C16612 .
  
  lld:C0085083 a ncit:C7057 .
  
  dgn-gda:DGN69a2053fb94aa6173b54aef1fef2ca9e sio:SIO_000628 miriam-gene:6046, lld:C0085083;
    a sio:SIO_001121 .
}

dgn-np:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_provenance {
  dgn-np:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_assertion dcterms:description
      "[Beside point mutations, FSHR gene polymorphisms at specific sites (e.g., codons 307 and 680) may influence FSHR protein responsiveness to exogenous FSH, and finally affect the effectiveness of in vitro fertilization (IVF) treatment as well as the likelihood of developing a severe OHSS as a consequence of superovulation.]. 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:19017414;
    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:NP499308.RAAB0s-lW0bc1lynW2tDESa9YTS8UnOKl_Lq7cYzI9xIA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:57+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" .
}