@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E> .
@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:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_head {
  this: np:hasAssertion dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_assertion ;
    np:hasProvenance dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_provenance ;
    np:hasPublicationInfo dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_assertion a np:Assertion .
  dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_provenance a np:Provenance .
  dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_assertion {
  miriam-gene:7043 a ncit:C16612 .
  lld:C0349788 a ncit:C7057 .
  dgn-gda:DGN072fd44428548651f57034a407c18f7d sio:SIO_000628 miriam-gene:7043 , lld:C0349788 ;
    a sio:SIO_001121 .
}
dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_provenance {
  dgn-np:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_assertion dcterms:description "[Direct sequencing of DNA from individuals belonging to established ARVD1 families failed to detect causative mutations in exonic sequences of four genes (POMT2, TGFbeta3, KIAAA1036 and KIAA0759) expressed in the heart and which defects could possibly induce plasma membrane instability or apoptosis, key features of ARVD pathogenesis.]. 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:12529708 ;
    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:NP523223.RAFJlEusD72oFY5tRfg8DbCmWmMBOZedijJBEEMu29_6E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:11+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" .
}