@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk> .
@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:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_head {
  this: np:hasAssertion dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_assertion;
    np:hasProvenance dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_provenance;
    np:hasPublicationInfo dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_assertion a np:Assertion .
  
  dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_provenance a np:Provenance .
  
  dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_assertion {
  miriam-gene:3953 a ncit:C16612 .
  
  lld:C0018801 a ncit:C7057 .
  
  dgn-gda:DGNa869e09fe552a90c52a17b2dc67ad274 sio:SIO_000628 miriam-gene:3953, lld:C0018801;
    a sio:SIO_001122 .
}

dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_provenance {
  dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_assertion dcterms:description
      "[The aim of this study was to investigate the possible associations of defined variability in leptin (dbSNP ID rs7799039), proopiomelanocortin (dbSNP ID rs3754860 and dbSNP ID rs1009388), and leptin receptor gene (dbSNP rs1137101) with CHF and evaluate their potential as the CHF susceptibility genes.]. 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:19337797;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:34+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" .
}