@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ> .
@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:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_head {
  this: np:hasAssertion dgn-np:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_assertion;
    np:hasProvenance dgn-np:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_provenance;
    np:hasPublicationInfo dgn-np:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_assertion a np:Assertion .
  
  dgn-np:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_provenance a np:Provenance .
  
  dgn-np:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_assertion {
  miriam-gene:2688 a ncit:C16612 .
  
  lld:C0028326 a ncit:C7057 .
  
  dgn-gda:DGN0786a0083843f8d60206c112918c400b sio:SIO_000628 miriam-gene:2688, lld:C0028326;
    a sio:SIO_001121 .
}

dgn-np:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_provenance {
  dgn-np:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_assertion dcterms:description
      "[The objective of this study was to evaluate the efficacy of recombinant human growth hormone (rhGH) therapy and the influence of genotype on the response to rhGH therapy in children with Noonan syndrome (NS).]. 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:22777296;
    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:NP551906.RAA59yadpvaQaNn2v1zr358iBYVDIhOdSQTWHxq_PGFmQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:33+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" .
}