@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o> .
@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:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_head {
  this: np:hasAssertion dgn-np:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_assertion;
    np:hasProvenance dgn-np:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_provenance;
    np:hasPublicationInfo dgn-np:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_assertion a np:Assertion .
  
  dgn-np:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_provenance a np:Provenance .
  
  dgn-np:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_assertion {
  miriam-gene:5339 a ncit:C16612 .
  
  lld:C0026850 a ncit:C7057 .
  
  dgn-gda:DGN12daf332f3c3e32bf12c4161e0203ef7 sio:SIO_000628 miriam-gene:5339, lld:C0026850;
    a sio:SIO_001121 .
}

dgn-np:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_provenance {
  dgn-np:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_assertion dcterms:description
      "[Because plectin deficiency is associated with muscular dystrophy, molecular diagnostics of the plectin gene provides prognostic value in evaluation of these patients who appear to be at risk to develop muscular dystrophy.]. 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:10652002;
    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:NP263991.RA48dPJLoTU5jJ3XzgSCrDAuKx2UBBjLLcjNgscReYN3o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:27+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" .
}