@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0> .
@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:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_head {
  this: np:hasAssertion dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_assertion;
    np:hasProvenance dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_provenance;
    np:hasPublicationInfo dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_assertion a np:Assertion .
  
  dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_provenance a np:Provenance .
  
  dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0007193 a ncit:C7057 .
  
  dgn-gda:DGN2112173d0515f01a305d0e26740fba5f sio:SIO_000628 miriam-gene:4000, lld:C0007193;
    a sio:SIO_001122 .
}

dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_provenance {
  dgn-np:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_assertion dcterms:description
      "[The study documents that D192G mutation in LMNA gene may lead to the disruption of the nuclear wall in cardiomyocytes, thus supporting the mechanical hypothesis of dilated cardiomyopathy development in humans, which might be mutation-specific.]. 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:18502446;
    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:NP673076.RAjCT4JReUyCucT92X66i7mhK4YYqorzEob214QUiZsy0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:50+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: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" .
}