@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8> .
@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:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_head {
  this: np:hasAssertion dgn-np:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_assertion;
    np:hasProvenance dgn-np:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_provenance;
    np:hasPublicationInfo dgn-np:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_assertion a np:Assertion .
  
  dgn-np:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_provenance a np:Provenance .
  
  dgn-np:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_assertion {
  miriam-gene:2254 a ncit:C16612 .
  
  lld:C0018051 a ncit:C7057 .
  
  dgn-gda:DGNc9081e0d6665786186bc90c9fcc2e4dd sio:SIO_000628 miriam-gene:2254, lld:C0018051;
    a sio:SIO_001121 .
}

dgn-np:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_provenance {
  dgn-np:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_assertion dcterms:description
      "[In this study, we systematically screened sequences of the FGF9 gene in 21 XY females and 72 XX females and XY males to examine whether sequence variants of the FGF9 gene play a pathophysiological role on human gonadal dysgenesis.]. 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:17154280;
    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:NP351479.RABDgPBorYY72RG5N4BOlzoEI68u245oy63tnTxAvm6I8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:26+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" .
}