@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4> .
@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:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_head {
  this: np:hasAssertion dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_assertion;
    np:hasProvenance dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_provenance;
    np:hasPublicationInfo dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_assertion a np:Assertion .
  
  dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_provenance a np:Provenance .
  
  dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0004153 a ncit:C7057 .
  
  dgn-gda:DGN98d0b5bb94f147a080499ae2628e01c3 sio:SIO_000628 miriam-gene:4000, lld:C0004153;
    a sio:SIO_001121 .
}

dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_provenance {
  dgn-np:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_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-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:NP485864.RAOz-tl5Rn4hX9uAE4o0vNounLL_YqQKwXD-KVyOgQlk4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:50+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" .
}