@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4> .
@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:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_head {
  this: np:hasAssertion dgn-np:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_assertion;
    np:hasProvenance dgn-np:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_provenance;
    np:hasPublicationInfo dgn-np:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_assertion a np:Assertion .
  
  dgn-np:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_provenance a np:Provenance .
  
  dgn-np:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_assertion {
  miriam-gene:825 a ncit:C16612 .
  
  lld:C0686353 a ncit:C7057 .
  
  dgn-gda:DGNe66e1a987c171f20051f53059db779e5 sio:SIO_000628 miriam-gene:825, lld:C0686353;
    a sio:SIO_001122 .
}

dgn-np:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_provenance {
  dgn-np:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_assertion dcterms:description
      "[Study provides evidence of the pathogenetic effect of specific CAPN3 gene mutations on protein function in limb girdle muscular dystrophy type 2A muscle and offers insights into the protein regions that are crucial for the autolytic activity of calpain-3.]. 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:16971480;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP145436.RAqKL2ZfgQvC_DT6U54TpDykHhirm6ml5-w51302iGvO4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:16+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" .
}