@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c> .
@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/v3.0.0/void/> .

dgn-np:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_head {
  this: np:hasAssertion dgn-np:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_assertion;
    np:hasProvenance dgn-np:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_provenance;
    np:hasPublicationInfo dgn-np:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_assertion a np:Assertion .
  
  dgn-np:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_provenance a np:Provenance .
  
  dgn-np:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_assertion {
  miriam-gene:3730 a ncit:C16612 .
  
  lld:C0020619 a ncit:C7057 .
  
  dgn-gda:DGN1da1b5049433582e3cec5b57163d0ec2 sio:SIO_000628 miriam-gene:3730, lld:C0020619;
    a sio:SIO_001122 .
}

dgn-np:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_provenance {
  dgn-np:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_assertion dcterms:description
      "[Rare variants in genes associated with idiopathic hypogonadotropic hypogonadism are found in women with hypothalamic amenorrhea, suggesting that these mutations may contribute to the variable susceptibility of women to the functional changes in GnRH secre]. 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:21247312;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP97199.RA1Ry2lqrkfVMAC52rdghBj21Wq6D3-7iQbbjpll7eu_c130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:33+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}