@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4> .
@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:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_head {
  this: np:hasAssertion dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_assertion;
    np:hasProvenance dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_provenance;
    np:hasPublicationInfo dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_assertion a np:Assertion .
  
  dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_provenance a np:Provenance .
  
  dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_assertion {
  miriam-gene:5741 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGN15bb668abc376754b9f7184e21117fc7 sio:SIO_000628 miriam-gene:5741, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_provenance {
  dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_assertion dcterms:description
      "[We suggest that sustained stimulation of PTH receptors present in brain, muscle, and hematopoietic cells have to be considered as one independent, important cause of molecular disease in PHPT leading to profound alterations in gene expression that may help explain symptoms like muscle fatigue, cardiovascular pathology, and precipitation of psychiatric illness.]. 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:17227961;
    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:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:54+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" .
}