@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I> .
@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:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_head {
  this: np:hasAssertion dgn-np:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_assertion ;
    np:hasProvenance dgn-np:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_provenance ;
    np:hasPublicationInfo dgn-np:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_assertion a np:Assertion .
  dgn-np:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_provenance a np:Provenance .
  dgn-np:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  lld:C2936858 a ncit:C7057 .
  dgn-gda:DGNd1212730bc55b4edb083d5e4de31ab24 sio:SIO_000628 miriam-gene:3630 , lld:C2936858 ;
    a sio:SIO_001121 .
}
dgn-np:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_provenance {
  dgn-np:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_assertion dcterms:description "[A number of physiological alterations in the endocrine milieu at puberty, which include alterations in the growth hormone/insulin-like growth factor axis, insulin sensitivity, as well as the activity of enzymes participating in cortisol metabolism and adrenal steroidogenesis, may account for the documented hypocortisolism and elevated androgen production, and may explain the difficulty in maintaining adequate adrenocortical suppression in pubertal patients with classical 21-hydroxylase deficiency.]. 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:11919101 ;
    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:NP897556.RAKC6r2ew6XpYNTlglTZXKub_RpCx6srVugRjm5Q9nv0I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:11+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" .
}