@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4> .
@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:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_head {
  this: np:hasAssertion dgn-np:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_assertion;
    np:hasProvenance dgn-np:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_provenance;
    np:hasPublicationInfo dgn-np:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_assertion a np:Assertion .
  
  dgn-np:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_provenance a np:Provenance .
  
  dgn-np:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_assertion {
  miriam-gene:148 a ncit:C16612 .
  
  lld:C2937421 a ncit:C7057 .
  
  dgn-gda:DGN5022a52abb83788a6b5a2f2a158e4415 sio:SIO_000628 miriam-gene:148, lld:C2937421;
    a sio:SIO_001122 .
}

dgn-np:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_provenance {
  dgn-np:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_assertion dcterms:description
      "[In men with a clinical diagnosis of benign prostatic hyperplasia (BPH), polytomous logistic regression analysis was conducted to evaluate associations between two silent polymorphisms in SRD5A1 (codon positions 30 and 116), two polymorphisms in SRD5A2 (Val89Leu substitution and C to T transition in intron 1), a trinucleotide (CAG)n repeat in androgen receptor (AR), and an Arg492Cys substitution in ADRA1A and clinical parameters that characterize severity of BPH.]. 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:15136785;
    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:NP49159.RAAFCYI8WphA4KFOk5hdWBeXhAxbHql0RseMhkxwPmYI4130_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" .
}