@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc> .
@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:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_head {
  this: np:hasAssertion dgn-np:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_assertion;
    np:hasProvenance dgn-np:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_provenance;
    np:hasPublicationInfo dgn-np:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_assertion a np:Assertion .
  
  dgn-np:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_provenance a np:Provenance .
  
  dgn-np:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_assertion {
  miriam-gene:2692 a ncit:C16612 .
  
  lld:C0271563 a ncit:C7057 .
  
  dgn-gda:DGN32d8eed00dcd3c99dcce7e04de16b2be sio:SIO_000628 miriam-gene:2692, lld:C0271563;
    a sio:SIO_001121 .
}

dgn-np:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_provenance {
  dgn-np:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_assertion dcterms:description
      "[Whereas mutations in the GH-1 and GHRHR genes account for the majority of mutations detectable in patients with Isolated Growth Hormone Deficiency (IGHD) resulting in postnatal growth failure, the overall detection of genetic defects in these patients remains low with app.]. 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:22423511;
    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:NP737325.RAdqbid8-6w2KDL9MeOxzbSVN1td5D03EctzmfzZw_uZc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:27+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" .
}