@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c> .
@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/v4.0.0/void/> .

dgn-np:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_head {
  this: np:hasAssertion dgn-np:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_assertion;
    np:hasProvenance dgn-np:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_provenance;
    np:hasPublicationInfo dgn-np:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_assertion a np:Assertion .
  
  dgn-np:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_provenance a np:Provenance .
  
  dgn-np:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0035078 a ncit:C7057 .
  
  dgn-gda:DGN541f06778c2c361ad15e2ca1dc10f7e1 sio:SIO_000628 miriam-gene:1636, lld:C0035078;
    a sio:SIO_001121 .
}

dgn-np:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_provenance {
  dgn-np:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_assertion dcterms:description
      "[The ADD genotype is predictive of the course of renal function loss in an unselected renal population and influences the effect of the ACE genotype to modulate the rate of progression to ESRD.]. 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:11918733;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP349627.RAoCZ0x5ch8cEB2aImpCSmnTEyHsw7HZmONaJPORG5W4c130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:23+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}