@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k> .
@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:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_head {
  this: np:hasAssertion dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_assertion;
    np:hasProvenance dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_provenance;
    np:hasPublicationInfo dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_assertion a np:Assertion .
  
  dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_provenance a np:Provenance .
  
  dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_assertion {
  miriam-gene:2688 a ncit:C16612 .
  
  lld:C0744483 a ncit:C7057 .
  
  dgn-gda:DGNfb0f06bdb60c1083a685bad7e14daf90 sio:SIO_000628 miriam-gene:2688, lld:C0744483;
    a sio:SIO_001121 .
}

dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_provenance {
  dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_assertion dcterms:description
      "[We report a boy with anhidrotic/hypohidrotic ectodermal dysplasia and growth hormone neurosecretory dysfunction, an association not previously reported, and we discuss the possible causes as well as the patient's response to growth hormone treatment until he reached final height.]. 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:19960895;
    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:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:55+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" .
}