@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ> .
@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:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_head {
  this: np:hasAssertion dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_assertion;
    np:hasProvenance dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_provenance;
    np:hasPublicationInfo dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_assertion a np:Assertion .
  
  dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_provenance a np:Provenance .
  
  dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGN2ba9847d25513249f930aed827941fb2 sio:SIO_000628 miriam-gene:4000, lld:C0524620;
    a sio:SIO_001121 .
}

dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_provenance {
  dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_assertion dcterms:description
      "[One form of lipodystrophy, namely Dunnigan-type familial partial lipodystrophy (FPLD) was shown to result from mutations in the LMNA gene, which encodes nuclear lamins A and C. Although the relationship between the mutations in the nuclear envelope and insulin resistance is unclear at present, these findings might eventually be shown to have relevance for the common insulin resistance syndrome and for drug-associated lipodystrophies.]. 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:11286783;
    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:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+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" .
}