@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY> .
@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:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_head {
  this: np:hasAssertion dgn-np:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_assertion ;
    np:hasProvenance dgn-np:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_provenance ;
    np:hasPublicationInfo dgn-np:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_assertion a np:Assertion .
  dgn-np:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_provenance a np:Provenance .
  dgn-np:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_assertion {
  miriam-gene:5443 a ncit:C16612 .
  lld:C0001627 a ncit:C7057 .
  dgn-gda:DGN1bbf801ac55736dc15b51fd3ae910448 sio:SIO_000628 miriam-gene:5443 , lld:C0001627 ;
    a sio:SIO_001121 .
}
dgn-np:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_provenance {
  dgn-np:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_assertion dcterms:description "[The hormonal responses to ACTH of the family members with cryptic 21-hydroxylase deficiency were determined and compared to the responses of patients with CAH, patients with acquired adrenal hyperplasia, family members predicted to be heterozygous for CAH, family members predicted to be unaffected, and the general population.]. 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:6271801 ;
    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:NP293091.RANSbaQ8gz5FO693WtKoxO6XYy2CGVf3wmOuG1xyRxKGY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:46+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" .
}