@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8> .
@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:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_head {
  this: np:hasAssertion dgn-np:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_assertion;
    np:hasProvenance dgn-np:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_provenance;
    np:hasPublicationInfo dgn-np:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_assertion a np:Assertion .
  
  dgn-np:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_provenance a np:Provenance .
  
  dgn-np:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_assertion {
  miriam-gene:5741 a ncit:C16612 .
  
  lld:C0035078 a ncit:C7057 .
  
  dgn-gda:DGN801f4917845818d94d7556f47b8e595c sio:SIO_000628 miriam-gene:5741, lld:C0035078;
    a sio:SIO_001121 .
}

dgn-np:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_provenance {
  dgn-np:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_assertion dcterms:description
      "[Primary hyperparathyroidism (pHPT) is characterized by excessive production of parathyroid hormone (PTH) due to parathyroid adenomas while uremic secondary HPT (sHPT) is caused by parathyroid hyperplasia in response to renal failure.]. 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:12444900;
    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:NP836895.RA-3qTBTCRDSI6oXwJN9B7s1ixgdyJdJYWgu6-Za6UPB8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:32+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" .
}