@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q> .
@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 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:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_head {
  this: np:hasAssertion dgn-np:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_assertion;
    np:hasProvenance dgn-np:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_provenance;
    np:hasPublicationInfo dgn-np:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_assertion a np:Assertion .
  
  dgn-np:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_provenance a np:Provenance .
  
  dgn-np:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_assertion {
  miriam-gene:6751 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN56c8556fba2356134cf547c60b363e5f sio:SIO_000628 miriam-gene:6751, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_provenance {
  dgn-np:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_assertion dct:description
      "[Our results suggest that genetic variation in the SSTR5 gene and, particularly, the rs4988483 single nucleotide polymorphism influence circulating IGFI and IGFBP3 hormone levels with no measurable effect on prostate cancer risk.]. 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:19423539;
    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:NP81196.RAymVXYbP9QUZ5ddk8V1C5LIU-ElnAfpAY4b40qn7ut0Q130_publicationInfo {
  this: dct:created "2014-10-02T12:32:40+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}