@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y> .
@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:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_head {
  this: np:hasAssertion dgn-np:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_assertion;
    np:hasProvenance dgn-np:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_provenance;
    np:hasPublicationInfo dgn-np:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_assertion a np:Assertion .
  
  dgn-np:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_provenance a np:Provenance .
  
  dgn-np:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0023787 a ncit:C7057 .
  
  dgn-gda:DGN9021625ed4ab43b476c64e98305435d9 sio:SIO_000628 miriam-gene:4000, lld:C0023787;
    a sio:SIO_001121 .
}

dgn-np:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_provenance {
  dgn-np:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_assertion dcterms:description
      "[Previous studies have suggested that LMNA mutations 5' to the nuclear localization signal (NLS) are more likely to underlie laminopathies with cardiac or skeletal muscle involvement, while mutations 3' to the NLS are more likely to underlie lipodystrophy and progeroid syndromes.]. 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:18031308;
    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:NP169480.RAjRmWqhNr5AcONp4nrqeo7r5LQAC7UsSUQqDvVn-_l0Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}