@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c> .
@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:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_head {
  this: np:hasAssertion dgn-np:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_assertion;
    np:hasProvenance dgn-np:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_provenance;
    np:hasPublicationInfo dgn-np:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_assertion a np:Assertion .
  
  dgn-np:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_provenance a np:Provenance .
  
  dgn-np:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_assertion {
  miriam-gene:960 a ncit:C16612 .
  
  lld:C0729353 a ncit:C7057 .
  
  dgn-gda:DGNaa15febbf73e87f6f22a69ea90bbd20b sio:SIO_000628 miriam-gene:960, lld:C0729353;
    a sio:SIO_001121 .
}

dgn-np:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_provenance {
  dgn-np:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_assertion dcterms:description
      "[delayed puberty), but also many unexpected findings have been made, including the lack of phenotype in women with activating LHR mutations, and the discrepancy in phenotypes of men with inactivating mutations of FSHbeta (azoospermia and infertility) and FSHR (oligozoospermia and subfertility).]. 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:16730882;
    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:NP254026.RAfVVqMW4yD-uHoYSStqOBqUXeDcBg_YrkZD20_My2Y2c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:22+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" .
}