@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE> .
@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:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_head {
  this: np:hasAssertion dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_assertion;
    np:hasProvenance dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_provenance;
    np:hasPublicationInfo dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_assertion a np:Assertion .
  
  dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_provenance a np:Provenance .
  
  dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_assertion {
  miriam-gene:2688 a ncit:C16612 .
  
  lld:C0013336 a ncit:C7057 .
  
  dgn-gda:DGNcf4cb7c3f8a77413c96f733c5318596c sio:SIO_000628 miriam-gene:2688, lld:C0013336;
    a sio:SIO_001121 .
}

dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_provenance {
  dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_assertion dcterms:description
      "[These results indicate that GH deficiency may contribute to short stature in children with Bartter syndrome, and rhGH therapy would be an excellent adjunctive treatment for short children with this syndrome whose condition is resistant to conventional therapies in terms of growth.]. 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:22707176;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:46+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" .
}