@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w> .
@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:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_head {
  this: np:hasAssertion dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_assertion;
    np:hasProvenance dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_provenance;
    np:hasPublicationInfo dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_assertion a np:Assertion .
  
  dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_provenance a np:Provenance .
  
  dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_assertion {
  miriam-gene:5444 a ncit:C16612 .
  
  lld:C0004153 a ncit:C7057 .
  
  dgn-gda:DGN1ce2fbad7c5395a65f9012b7ab1bd945 sio:SIO_000628 miriam-gene:5444, lld:C0004153;
    a sio:SIO_001122 .
}

dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_provenance {
  dgn-np:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_assertion dcterms:description
      "[A common polymorphism in the PON gene (PON1) causes an amino acid substitution of methionine (M) for leucine (L) at position 55 in the protein, which changes the activity of PON and can affect the risk of atherosclerosis.]. 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:11555845;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP52928.RARHWlWvSPat_vdUcbG4ubqCuxf3D34En9zGtzONWbb1w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}