@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI> .
@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/v4.0.0/void/> .

dgn-np:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_head {
  this: np:hasAssertion dgn-np:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_assertion;
    np:hasProvenance dgn-np:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_provenance;
    np:hasPublicationInfo dgn-np:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_assertion a np:Assertion .
  
  dgn-np:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_provenance a np:Provenance .
  
  dgn-np:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_assertion {
  miriam-gene:5376 a ncit:C16612 .
  
  lld:C0270922 a ncit:C7057 .
  
  dgn-gda:DGN318eddcba955ee66e430828b2ffabd70 sio:SIO_000628 miriam-gene:5376, lld:C0270922;
    a sio:SIO_001121 .
}

dgn-np:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_provenance {
  dgn-np:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_assertion dcterms:description
      "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. 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:18663734;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:55+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>,
      <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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}