@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w> .
@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:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_head {
  this: np:hasAssertion dgn-np:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_assertion;
    np:hasProvenance dgn-np:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_provenance;
    np:hasPublicationInfo dgn-np:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_assertion a np:Assertion .
  
  dgn-np:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_provenance a np:Provenance .
  
  dgn-np:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_assertion {
  miriam-gene:2688 a ncit:C16612 .
  
  lld:C0001206 a ncit:C7057 .
  
  dgn-gda:DGN24c0184404c13cde4daa5867af7ad715 sio:SIO_000628 miriam-gene:2688, lld:C0001206;
    a sio:SIO_001121 .
}

dgn-np:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_provenance {
  dgn-np:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_assertion dcterms:description
      "[Those that cause growth hormone (GH) excess and acromegaly are subdivided into morphologic variants that have not yet been shown to have pathogenetic significance or predictive value for therapy and outcome.]. 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:17671221;
    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:NP261206.RAsMpM3wH4jMGPFCrDS4l2CBPjnehppzemejbEbYzMS5w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}