@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8> .
@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:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_head {
  this: np:hasAssertion dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_assertion;
    np:hasProvenance dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_provenance;
    np:hasPublicationInfo dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_assertion a np:Assertion .
  
  dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_provenance a np:Provenance .
  
  dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_assertion {
  miriam-gene:80347 a ncit:C16612 .
  
  lld:C3494506 a ncit:C7057 .
  
  dgn-gda:DGN033d71087bb5fe28815d4b05aad5f649 sio:SIO_000628 miriam-gene:80347, lld:C3494506;
    a sio:SIO_001121 .
}

dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_provenance {
  dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_assertion dcterms:description
      "[Classically, patients with PHP have the skeletal features of AHO, resistance to multiple hormones that work via cAMP such as parathyroid hormone and thyroid stimulating hormone, and deficient activity of Gs protein, the guanine nucleotide-binding protein that stimulates adenylate cyclase.]. 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:1621772;
    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:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:42+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" .
}