@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s> .
@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:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_head {
  this: np:hasAssertion dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_assertion;
    np:hasProvenance dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_provenance;
    np:hasPublicationInfo dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_assertion a np:Assertion .
  
  dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_provenance a np:Provenance .
  
  dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNde1ae52af80b7b860bf349ac1a799ba7 sio:SIO_000628 miriam-gene:3949, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_provenance {
  dgn-np:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_assertion dcterms:description
      "[An improved understanding of etiologically complex pathologies involving the interplay of genes and the environment, such as atherosclerosis and systemic hypertension, has led to the identification of new targets for gene therapy, with the potential to alleviate inherited genetic defects such as familial hypercholesterolemia.]. 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:11711525;
    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:NP353886.RAArygvegp7xlnKDQk3pycABAg4bpb-ZAhJJSNHEYDn3s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:27+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}