@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_head {
  this: np:hasAssertion dgn-np:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_assertion;
    np:hasProvenance dgn-np:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_provenance;
    np:hasPublicationInfo dgn-np:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_assertion a np:Assertion .
  
  dgn-np:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_provenance a np:Provenance .
  
  dgn-np:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_assertion {
  miriam-gene:51738 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGN237c071df33d25ca6638db2683360164 sio:SIO_000628 miriam-gene:51738, lld:C0011847;
    a sio:SIO_001121 .
}

dgn-np:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_provenance {
  dgn-np:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_assertion dcterms:description
      "[In the present study we genotyped six variants of the ghrelin gene and its promoter, and tested whether these single nucleotide polymorphisms (SNPs) were associated with BP levels in participants of the Finnish Diabetes Prevention Study.]. 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:16942934;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP907799.RAFVn9DOC7jakr2rHc6-RVkHpxn_bSKc0Mb6oHhjQxu9U130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:54+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}