@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_head {
  this: np:hasAssertion dgn-np:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_assertion;
    np:hasProvenance dgn-np:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_provenance;
    np:hasPublicationInfo dgn-np:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_assertion a np:Assertion .
  
  dgn-np:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_provenance a np:Provenance .
  
  dgn-np:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_assertion {
  miriam-gene:5827 a ncit:C16612 .
  
  lld:C3714552 a ncit:C7057 .
  
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dgn-np:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_provenance {
  dgn-np:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_assertion dcterms:description
      "[Most importantly, we did not observe any correlation between PMP22 messenger RNA levels and the different clinical and electrophysiological outcome measures, underscoring the weakness of PMP22 to mirror the phenotypic variability of patients with CMT1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP662300.RAldLsoHNY_vYo6Tjy9q9KFbbk5LUFU81q8hsbibFhgP8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:18+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:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}