@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo> .
@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:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_head {
  this: np:hasAssertion dgn-np:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_assertion;
    np:hasProvenance dgn-np:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_provenance;
    np:hasPublicationInfo dgn-np:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_assertion a np:Assertion .
  
  dgn-np:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_provenance a np:Provenance .
  
  dgn-np:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_assertion {
  miriam-gene:5741 a ncit:C16612 .
  
  lld:C0020437 a ncit:C7057 .
  
  dgn-gda:DGN633d00d7c4b040dfbf5442efec34a264 sio:SIO_000628 miriam-gene:5741, lld:C0020437;
    a sio:SIO_001121 .
}

dgn-np:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_provenance {
  dgn-np:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_assertion dcterms:description
      "[Familial benign hypercalcemia results from the inappropriate secretion of parathyroid hormone despite hypercalcemia, enhanced renal tubular reabsorption of calcium (independent of parathyroid hormone), and apparent tissue resistance to adverse effects of hypercalcemia.]. 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:8053177;
    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:NP267795.RAajgeGKR9zStqnUWDgMoiCeSa2GYzw_qOB6I7rxwAWOo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:29+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" .
}