@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA> .
@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:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_head {
  this: np:hasAssertion dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_assertion;
    np:hasProvenance dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_provenance;
    np:hasPublicationInfo dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_assertion a np:Assertion .
  
  dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_provenance a np:Provenance .
  
  dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_assertion {
  miriam-gene:5449 a ncit:C16612 .
  
  lld:C0599750 a ncit:C7057 .
  
  dgn-gda:DGNa6fd43e480c0b88f4088041eddf4dd87 sio:SIO_000628 miriam-gene:5449, lld:C0599750;
    a sio:SIO_001121 .
}

dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_provenance {
  dgn-np:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_assertion dcterms:description
      "[Mutations in Prophet of PIT1 (Prop1), one of several homeodomain transcription factors that are required for the development of the anterior pituitary gland, are the predominant cause of MPHD (multiple pituitary hormone deficiency) in humans.]. 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:15459176;
    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:NP471755.RAPIgVspy9HH328yaXQDExdqJ8vPI-kAkE4g78uBQ7knA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:43+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" .
}