@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo> .
@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:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_head {
  this: np:hasAssertion dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_assertion ;
    np:hasProvenance dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_provenance ;
    np:hasPublicationInfo dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_assertion a np:Assertion .
  dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_provenance a np:Provenance .
  dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  lld:C0004245 a ncit:C7057 .
  dgn-gda:DGNae7ca2f1da155e55c0f014616387bf5f sio:SIO_000628 miriam-gene:4000 , lld:C0004245 ;
    a sio:SIO_001121 .
}
dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_provenance {
  dgn-np:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_assertion dcterms:description "[Even though mutations in LMNA have been reported in patients with typical dilated cardiomyopathy (DCM) and atrioventricular block (AVB) previously, the purpose of this study was to disclose this novel genetic abnormality in one Chinese family with the atypical phenotype of progressive AVB followed by DCM with normal QRS interval.]. 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:20155465 ;
    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:NP321065.RAacDfE9Xk7icu9EJ-3GK-Kd-wk9FzP_W_M-XCeq9Y_zo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:06+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" .
}