@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU> .
@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:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_head {
  this: np:hasAssertion dgn-np:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_assertion;
    np:hasProvenance dgn-np:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_provenance;
    np:hasPublicationInfo dgn-np:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_assertion a np:Assertion .
  
  dgn-np:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_provenance a np:Provenance .
  
  dgn-np:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_assertion {
  miriam-gene:3767 a ncit:C16612 .
  
  lld:C2931834 a ncit:C7057 .
  
  dgn-gda:DGNe510a367a929ff44f93355581e12bb4f sio:SIO_000628 miriam-gene:3767, lld:C2931834;
    a sio:SIO_001122 .
}

dgn-np:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_provenance {
  dgn-np:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_assertion dcterms:description
      "[In this large series, HNF4A mutations are the third most common cause of diazoxide responsive HH. We recommend that HNF4A sequencing is considered in all patients with diazoxide responsive HH diagnosed in the first week of life irrespective of a family hi]. 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:20164212;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP70206.RALocHr3iFoCuqi0YuK0VWLiihFs6R5M7BS6308ABV9WU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:18+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" .
}