@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc> .
@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:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_head {
  this: np:hasAssertion dgn-np:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_assertion ;
    np:hasProvenance dgn-np:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_provenance ;
    np:hasPublicationInfo dgn-np:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_assertion a np:Assertion .
  dgn-np:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_provenance a np:Provenance .
  dgn-np:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_assertion {
  miriam-gene:84467 a ncit:C16612 .
  lld:C0032460 a ncit:C7057 .
  dgn-gda:DGN724546e77a6907739e07cadb7513e017 sio:SIO_000628 miriam-gene:84467 , lld:C0032460 ;
    a sio:SIO_001121 .
}
dgn-np:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_provenance {
  dgn-np:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_assertion dcterms:description "[In an attempt to evaluate the association between allele 8 (A8) of D19S884 in the fibrillin-3 gene and circulating transforming growth factor (TGF) β and inhibin levels in women with polycystic ovary syndrome (PCOS), we studied 120 similarly aged women from families with PCOS and compared 40 women with PCOS who did not have A8 (A8- PCOS) with 40 women with PCOS who had A8 (A8+ PCOS) and 40 normally menstruating women who did not have either PCOS or A8 (A8- Non-PCOS).]. 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:20630504 ;
    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:NP682421.RA27jTn4x0scZTwTNgTKFqaIavveP5KCWJqleFDdPnIDc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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> ;
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}