@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg> .
@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:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_head {
  this: np:hasAssertion dgn-np:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_assertion;
    np:hasProvenance dgn-np:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_provenance;
    np:hasPublicationInfo dgn-np:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_assertion a np:Assertion .
  
  dgn-np:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_provenance a np:Provenance .
  
  dgn-np:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_assertion {
  miriam-gene:5827 a ncit:C16612 .
  
  lld:C0031117 a ncit:C7057 .
  
  dgn-gda:DGN5b41854b50c8f00db238d86e7cb2b73c sio:SIO_000628 miriam-gene:5827, lld:C0031117;
    a sio:SIO_001121 .
}

dgn-np:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_provenance {
  dgn-np:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_assertion dcterms:description
      "[Many myelin gene mutants that cause severe disease, such as those in the myelin protein zero gene (MPZ) and the peripheral myelin protein 22 gene (PMP22), appear to make aberrant proteins that accumulate primarily within the endoplasmic reticulum (ER), resulting in Schwann cell death by apoptosis and, subsequently, peripheral neuropathy.]. 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:17701891;
    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:NP526795.RA9u_qBp29p_LJ3-Kggmc1pIHik8Zm4kGZZfiBUr1sREg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:16+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" .
}