@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg> .
@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:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_head {
  this: np:hasAssertion dgn-np:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_assertion;
    np:hasProvenance dgn-np:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_provenance;
    np:hasPublicationInfo dgn-np:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_assertion a np:Assertion .
  
  dgn-np:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_provenance a np:Provenance .
  
  dgn-np:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_assertion {
  miriam-gene:2492 a ncit:C16612 .
  
  lld:C0021359 a ncit:C7057 .
  
  dgn-gda:DGN7c1bae72a50a8091df2ac4095fbb9d0b sio:SIO_000628 miriam-gene:2492, lld:C0021359;
    a sio:SIO_001121 .
}

dgn-np:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_provenance {
  dgn-np:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_assertion dcterms:description
      "[FSH receptor genotyping may, thus, be interesting as an adjunct indicator of ovarian reserve for infertile women undergoing assisted reproduction, and may be helpful in the determination of the starting dosage of FSH in in vitro fertilization.]. 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:16026410;
    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:NP336039.RAfgGE9Z0c6uG2x8n-BhO3HvxRVzPZ362KffOmxPGw9Qg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:17+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" .
}