@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk> .
@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:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_head {
  this: np:hasAssertion dgn-np:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_assertion;
    np:hasProvenance dgn-np:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_provenance;
    np:hasPublicationInfo dgn-np:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_assertion a np:Assertion .
  
  dgn-np:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_provenance a np:Provenance .
  
  dgn-np:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_assertion {
  miriam-gene:3569 a ncit:C16612 .
  
  lld:C0334121 a ncit:C7057 .
  
  dgn-gda:DGN6b42ef5abbad435c44f705e68b436f00 sio:SIO_000628 miriam-gene:3569, lld:C0334121;
    a sio:SIO_001121 .
}

dgn-np:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_provenance {
  dgn-np:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_assertion dcterms:description
      "[Some researchers have reported that IMT is high in people with functional variants of genes related to matrix deposition (MMP3), inflammation (interleukin 6), and lipid metabolism (hepatic lipase, APOE, CETP, and PON1).]. 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:15039035;
    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:NP423772.RADc57Skw2L5fycUhLWdpweoCCRWrbsq5Ce5OtBVUVPKk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:11+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" .
}