@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8> .
@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:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_head {
  this: np:hasAssertion dgn-np:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_assertion;
    np:hasProvenance dgn-np:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_provenance;
    np:hasPublicationInfo dgn-np:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_assertion a np:Assertion .
  
  dgn-np:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_provenance a np:Provenance .
  
  dgn-np:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_assertion {
  miriam-gene:6462 a ncit:C16612 .
  
  lld:C0600327 a ncit:C7057 .
  
  dgn-gda:DGNefe53f1f99eb9e54b6db611a225c16ab sio:SIO_000628 miriam-gene:6462, lld:C0600327;
    a sio:SIO_001121 .
}

dgn-np:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_provenance {
  dgn-np:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_assertion dcterms:description
      "[The identification of multiple transcription start sites (TSS) upstream of the annotated first exon of human SHBG, and the detection of the alternative transcripts in human prostate, concur with the prediction of the ENCODE (ENCyclopedia of DNA Elements) project, and suggest that the regulation of SHBG is much more complex than previously reported.]. 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:19534810;
    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:NP354302.RAjgNgiDXKQyjC-hD8I_gl0yT_iiV8ExqSqub7dmPfvo8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:28+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" .
}