@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM> .
@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:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_head {
  this: np:hasAssertion dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_assertion;
    np:hasProvenance dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_provenance;
    np:hasPublicationInfo dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_assertion a np:Assertion .
  
  dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_provenance a np:Provenance .
  
  dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_assertion {
  miriam-gene:2492 a ncit:C16612 .
  
  lld:C0021361 a ncit:C7057 .
  
  dgn-gda:DGNb4a2fda3d2a2c1f6a6aeafdbbc1fe811 sio:SIO_000628 miriam-gene:2492, lld:C0021361;
    a sio:SIO_001122 .
}

dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_provenance {
  dgn-np:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_assertion dcterms:description
      "[ The results show that Ser/Ser-680 predominates in the studied infertile population. Furthermore, women with normal ovarian reserve and the Ser/Ser FSH receptor variant had significantly higher FSH levels, compared to women with Asn/Asn and Asn/Ser variants. 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:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP43872.RA-f22YlqCUcZacThYOlwma5Z6xQNF7DrEL9ezCObmXaM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}