@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus> .
@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:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_head {
  this: np:hasAssertion dgn-np:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_assertion;
    np:hasProvenance dgn-np:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_provenance;
    np:hasPublicationInfo dgn-np:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_assertion a np:Assertion .
  
  dgn-np:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_provenance a np:Provenance .
  
  dgn-np:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_assertion {
  miriam-gene:6658 a ncit:C16612 .
  
  lld:C0476273 a ncit:C7057 .
  
  dgn-gda:DGN43973e51fb363b35729940b69c7db0df sio:SIO_000628 miriam-gene:6658, lld:C0476273;
    a sio:SIO_001121 .
}

dgn-np:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_provenance {
  dgn-np:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_assertion dcterms:description
      "[The objectives of the study were to describe the complex phenotype associated with the panhypopituitarism of two unrelated Italian patients who, at birth, presented with hypoglycemic seizures and respiratory distress complicated by shock, in a familial context of neonatal death in one family and spontaneous miscarriage in both families and to identify the molecular basis of this unusual syndrome.]. 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:16940453;
    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:NP237067.RA3BDM9HlqroYhHofVreGlJObhfil9JUGDXCWQitGDNus130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}