@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM> .
@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/v4.0.0/void/> .

dgn-np:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_head {
  this: np:hasAssertion dgn-np:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_assertion;
    np:hasProvenance dgn-np:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_provenance;
    np:hasPublicationInfo dgn-np:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_assertion a np:Assertion .
  
  dgn-np:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_provenance a np:Provenance .
  
  dgn-np:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_assertion {
  miriam-gene:2688 a ncit:C16612 .
  
  lld:C0032002 a ncit:C7057 .
  
  dgn-gda:DGNd34f20357d41bf290b95a421758c631c sio:SIO_000628 miriam-gene:2688, lld:C0032002;
    a sio:SIO_001123 .
}

dgn-np:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_provenance {
  dgn-np:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_assertion dcterms:description
      "[Mutations of the pituitary transcription factor gene POU1F1 (the human homologue of mouse Pit1) are responsible for deficiencies of GH, prolactin and thyroid stimulating hormone (TSH) in Snell and Jackson dwarf mice and in man, while the production of adrenocorticotrophic hormone (ACTH), luteinizing hormone (LH) and follicle stimulating hormone (FSH) is preserved.]. 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:9462743;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1388542.RA2o5jaycEbr11OP9tdvRWCASkxUvEbBOTHienf6NwNJM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:15+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}