@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw> .
@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:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_head {
  this: np:hasAssertion dgn-np:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_assertion;
    np:hasProvenance dgn-np:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_provenance;
    np:hasPublicationInfo dgn-np:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_assertion a np:Assertion .
  
  dgn-np:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_provenance a np:Provenance .
  
  dgn-np:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_assertion {
  miriam-gene:5179 a ncit:C16612 .
  
  lld:C0031511 a ncit:C7057 .
  
  dgn-gda:DGNdc515fef61ad6125bfe5bd63d63ffe7a sio:SIO_000628 miriam-gene:5179, lld:C0031511;
    a sio:SIO_001121 .
}

dgn-np:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_provenance {
  dgn-np:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_assertion dcterms:description
      "[Northern blot analysis, using a single-stranded human proenkephalin A antisense probe (cRNA), revealed the existence of two different proenkephalin A-like sequences in the human caudate nucleus and pheochromocytoma RNA extracts of approximately 1400 and 1000 nucleotides in length respectively, whereas no specific RNA bands could be detected in the cortex and only the 1400 nucleotide band was present in the cerebellum.]. 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:3207862;
    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:NP501645.RApPY_5MT6yVoXax0RLJNFcAFNhWe99tIvBE8CQ58RIuw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:59+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" .
}