@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k> .
@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:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_head {
  this: np:hasAssertion dgn-np:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_assertion;
    np:hasProvenance dgn-np:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_provenance;
    np:hasPublicationInfo dgn-np:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_assertion a np:Assertion .
  
  dgn-np:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_provenance a np:Provenance .
  
  dgn-np:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_assertion {
  miriam-gene:2688 a ncit:C16612 .
  
  lld:C0497552 a ncit:C7057 .
  
  dgn-gda:DGNdc62fa7ed7ffbc7bd0f70a40952355c3 sio:SIO_000628 miriam-gene:2688, lld:C0497552;
    a sio:SIO_001121 .
}

dgn-np:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_provenance {
  dgn-np:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_assertion dcterms:description
      "[When a child is not following the normal, predicted growth curve, an evaluation for underlying illnesses and central nervous system abnormalities is required, and appropriate consideration should be given to genetic defects causing growth hormone (GH) deficiency (GHD).]. 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:21274339;
    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:NP334508.RAPvjaPP64lhAWAkCnayOoGcofYwqHZe6xzK4Fwbt3J3k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:17+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" .
}