@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0> .
@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:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_head {
  this: np:hasAssertion dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_assertion ;
    np:hasProvenance dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_provenance ;
    np:hasPublicationInfo dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_assertion a np:Assertion .
  dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_provenance a np:Provenance .
  dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_assertion {
  miriam-gene:5626 a ncit:C16612 .
  lld:C0001403 a ncit:C7057 .
  dgn-gda:DGNd6d8c1a7b780ce715eca9ee12d2cc4ba sio:SIO_000628 miriam-gene:5626 , lld:C0001403 ;
    a sio:SIO_001121 .
}
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_provenance {
  dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_assertion dcterms:description "[In addition to GH, TSH, PRL and gonadotropin deficiency, patients with PROP-1 gene mutations can present with late-onset central hypocortisolism, possibly beause of the lack of important paracrine factors normally produced by the cells surrounding the corticotropes and absent in the pituitary of these patients, or because of progressive corticotrope apoptosis.]. 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:11022176 ;
    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:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:20+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" .
}