@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU> .
@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:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_head {
  this: np:hasAssertion dgn-np:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_assertion;
    np:hasProvenance dgn-np:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_provenance;
    np:hasPublicationInfo dgn-np:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_assertion a np:Assertion .
  
  dgn-np:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_provenance a np:Provenance .
  
  dgn-np:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_assertion {
  miriam-gene:11132 a ncit:C16612 .
  
  lld:C0032460 a ncit:C7057 .
  
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    a sio:SIO_001122 .
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dgn-np:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_provenance {
  dgn-np:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_assertion dcterms:description
      "[Our results confirm the association of UCSNP-44 allele with PCO phenotype in the Spanish population. Moreover, we have identified novel candidate risk alleles and genotypes, within CAPN10 gene, that could be associated with important phenotypic and prognosis differences observed in PCOS patients.]. 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:14602801;
    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:NP47648.RA0YxQvTTonpo03BK3IUjorb0LoOJOPbJvNsQgIHHjqnU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}