@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4> .
@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:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_head {
  this: np:hasAssertion dgn-np:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_assertion;
    np:hasProvenance dgn-np:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_provenance;
    np:hasPublicationInfo dgn-np:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_assertion a np:Assertion .
  
  dgn-np:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_provenance a np:Provenance .
  
  dgn-np:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_assertion {
  miriam-gene:645 a ncit:C16612 .
  
  lld:C0013336 a ncit:C7057 .
  
  dgn-gda:DGN18e8c16e6a7214747b517017e9750003 sio:SIO_000628 miriam-gene:645, lld:C0013336;
    a sio:SIO_001121 .
}

dgn-np:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_provenance {
  dgn-np:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_assertion dcterms:description
      "[Because it has been reported that non-22-kDa GH isoforms might be partly responsible for short stature and growth retardation in children, the aim of this study was to compare the impact of both 22 kDa and 20 kDa GH on GH receptor gene (GH receptor/GH binding protein (GHR/GHBP)) expression.]. 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:10810295;
    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:NP247837.RActxmaTt_9Is_OmhchQ0IwFKNhMBlanMy5J1GCb6Abi4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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: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" .
}