@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk> .
@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:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_head {
  this: np:hasAssertion dgn-np:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_assertion;
    np:hasProvenance dgn-np:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_provenance;
    np:hasPublicationInfo dgn-np:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_assertion a np:Assertion .
  
  dgn-np:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_provenance a np:Provenance .
  
  dgn-np:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_assertion {
  miriam-gene:270 a ncit:C16612 .
  
  lld:C0151744 a ncit:C7057 .
  
  dgn-gda:DGN5e4fc73f949c26154daa88f135875037 sio:SIO_000628 miriam-gene:270, lld:C0151744;
    a sio:SIO_001122 .
}

dgn-np:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_provenance {
  dgn-np:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_assertion dcterms:description
      "[Possession of the C34T mutation in AMP deaminase (AMPD1) gene has been shown to be associated with attenuation of the progression of heart failure and improved survival in ischemic heart disease.]. 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:16021915;
    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:NP237658.RAE89IPZ7TYTBcRcN8lZlWuzUTStr08JUPLO7sydGHrVk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:55+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" .
}