@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM> .
@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:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_head {
  this: np:hasAssertion dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_assertion;
    np:hasProvenance dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_provenance;
    np:hasPublicationInfo dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_assertion a np:Assertion .
  
  dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_provenance a np:Provenance .
  
  dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_assertion {
  miriam-gene:6046 a ncit:C16612 .
  
  lld:C0021364 a ncit:C7057 .
  
  dgn-gda:DGNf2e94a3784a8e86e1dd7c46abcfb16d2 sio:SIO_000628 miriam-gene:6046, lld:C0021364;
    a sio:SIO_001121 .
}

dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_provenance {
  dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_assertion dcterms:description
      "[To verify in another population (Italians) whether a single-nucleotide polymorphism in the FSHB gene promoter previously associated with serum FSH levels in Estonians is indeed associated with sperm count and FSH plasma levels, and especially to verify whether it could be a pharmacogenetic tool for the treatment of male infertility with FSH.]. 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:22000911;
    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:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:27+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" .
}