@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E> .
@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:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_head {
  this: np:hasAssertion dgn-np:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_assertion;
    np:hasProvenance dgn-np:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_provenance;
    np:hasPublicationInfo dgn-np:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_assertion a np:Assertion .
  
  dgn-np:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_provenance a np:Provenance .
  
  dgn-np:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_assertion {
  miriam-gene:64221 a ncit:C16612 .
  
  lld:C0004153 a ncit:C7057 .
  
  dgn-gda:DGN5241d9af942b8d6c0aa3cd30f5c5a2fb sio:SIO_000628 miriam-gene:64221, lld:C0004153;
    a sio:SIO_001121 .
}

dgn-np:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_provenance {
  dgn-np:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_assertion dcterms:description
      "[Although some common polymorphisms of LMNA have been associated with traits related to atherosclerosis, the monogenic diseases FPLD2 and HGPS are more likely to provide clues about new pathways for the general process 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:15205220;
    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:NP448743.RAEigBXuLhKmjinpRDihXCtp4dCOUAKi0nJkb7BlUCF6E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:08+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" .
}