@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU> .
@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:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_head {
  this: np:hasAssertion dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_assertion;
    np:hasProvenance dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_provenance;
    np:hasPublicationInfo dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_assertion a np:Assertion .
  
  dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_provenance a np:Provenance .
  
  dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_assertion {
  miriam-gene:8022 a ncit:C16612 .
  
  lld:C0599750 a ncit:C7057 .
  
  dgn-gda:DGNad7e8c34f75bfbd56a45d96bc411a185 sio:SIO_000628 miriam-gene:8022, lld:C0599750;
    a sio:SIO_001121 .
}

dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_provenance {
  dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_assertion dcterms:description
      "[All patients were homozygous, with various syndromic forms of combined pituitary hormone deficiency (CPHD), hampering to allocate, in these consanguineous patients, the respective contribution of LHX3 and additional genes to each symptom.]. 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:22238406;
    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:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:17+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" .
}