@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg> .
@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:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_head {
  this: np:hasAssertion dgn-np:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_assertion;
    np:hasProvenance dgn-np:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_provenance;
    np:hasPublicationInfo dgn-np:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_assertion a np:Assertion .
  
  dgn-np:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_provenance a np:Provenance .
  
  dgn-np:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_assertion {
  miriam-gene:5350 a ncit:C16612 .
  
  lld:C0007193 a ncit:C7057 .
  
  dgn-gda:DGNa6c0cfa276c62a165de35feb97313082 sio:SIO_000628 miriam-gene:5350, lld:C0007193;
    a sio:SIO_001121 .
}

dgn-np:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_provenance {
  dgn-np:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_assertion dcterms:description
      "[Interestingly, unlike other individuals reported with the identical PLN mutation, these individuals were not diagnosed with dilated cardiomyopathy until their seventh decade when they were only mildly symptomatic with congestive heart failure.]. 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:17010801;
    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:NP185053.RAa7T8-IicWAGTpMOw8eQVFZTVDvt_ahSiXCVLKC1-Wpg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:41+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" .
}