@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs> .
@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:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_head {
  this: np:hasAssertion dgn-np:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_assertion;
    np:hasProvenance dgn-np:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_provenance;
    np:hasPublicationInfo dgn-np:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_assertion a np:Assertion .
  
  dgn-np:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_provenance a np:Provenance .
  
  dgn-np:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_assertion {
  miriam-gene:5741 a ncit:C16612 .
  
  lld:C0033806 a ncit:C7057 .
  
  dgn-gda:DGN6afda6796755fc353869a6e6421439ca sio:SIO_000628 miriam-gene:5741, lld:C0033806;
    a sio:SIO_001121 .
}

dgn-np:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_provenance {
  dgn-np:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_assertion dcterms:description
      "[Recently, however, mutations in PRKAR1A, a regulatory subunit of the cAMP-dependent protein kinase, have been identified in several cases of PTH and other hormone resistance and skeletal dysplasia that are considered to be affected by PHP type II due to unimpaired urinary excretion of cAMP following PTH administration.]. 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:23392091;
    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:NP256782.RAnKue8YeSrPDPkBJwnLIam8KXqKBiBGkO1wzEACLBpWs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:23+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" .
}