@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU> .
@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:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_head {
  this: np:hasAssertion dgn-np:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_assertion;
    np:hasProvenance dgn-np:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_provenance;
    np:hasPublicationInfo dgn-np:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_assertion a np:Assertion .
  
  dgn-np:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_provenance a np:Provenance .
  
  dgn-np:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_assertion {
  miriam-gene:4878 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGNcfb93c2b59765757f8424ca2356f85d6 sio:SIO_000628 miriam-gene:4878, lld:C0038454;
    a sio:SIO_001121 .
}

dgn-np:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_provenance {
  dgn-np:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_assertion dcterms:description
      "[Two common single nucleotide polymorphisms (SNPs) in NPPA, rs5063 and rs5065, result in amino acid changes of the primary peptide and have been previously implicated in conditions associated with AF, including stroke and hypertension.]. 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:20543198;
    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:NP540584.RAnSyKPLkMxBVF4GjDrlfmwTFY42PIxTbAVeLEeEBKxDU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:26+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" .
}