@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8> .
@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:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_head {
  this: np:hasAssertion dgn-np:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_assertion;
    np:hasProvenance dgn-np:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_provenance;
    np:hasPublicationInfo dgn-np:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_assertion a np:Assertion .
  
  dgn-np:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_provenance a np:Provenance .
  
  dgn-np:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  
  lld:C0020502 a ncit:C7057 .
  
  dgn-gda:DGN48ae29210707437f80b40bd4eba89ffb sio:SIO_000628 miriam-gene:2099, lld:C0020502;
    a sio:SIO_001121 .
}

dgn-np:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_provenance {
  dgn-np:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_assertion dcterms:description
      "[Using conventional riboprobe in situ hybridization, ER transcripts were not detectable in any bone cells within sections taken from normal bone and several actively remodeling bone tissues, namely, Paget's disease, renal hyperparathyroidism, and healing fracture callus.]. 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:9028531;
    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:NP608815.RA6Cx_Av20-QzsPxyhGRLwfebO5x9esECrXFphs2d3MM8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:05+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" .
}