@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_head {
  this: np:hasAssertion dgn-np:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_assertion;
    np:hasProvenance dgn-np:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_provenance;
    np:hasPublicationInfo dgn-np:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_assertion a np:Assertion .
  
  dgn-np:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_provenance a np:Provenance .
  
  dgn-np:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_assertion {
  miriam-gene:6574 a ncit:C16612 .
  
  lld:C0020635 a ncit:C7057 .
  
  dgn-gda:DGNfc8346482b676c6e778281b9e9cd8e86 sio:SIO_000628 miriam-gene:6574, lld:C0020635;
    a sio:SIO_001121 .
}

dgn-np:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_provenance {
  dgn-np:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_assertion dcterms:description
      "[Diagnosing Pit-1 gene mutations as a rare cause of combined pituitary deficiency is important both for genetic counselling as well as for predicting the future course in the patient (spontaneous puberty, no glucocorticoid substitution necessary during stress periods).]. 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:9392393;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP701086.RAZwww56nx9L6PCA3Ntyp6OazmIr6pov7oOYU7-I0WkUY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:42+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}