@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ> .
@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:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_head {
  this: np:hasAssertion dgn-np:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_assertion;
    np:hasProvenance dgn-np:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_provenance;
    np:hasPublicationInfo dgn-np:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_assertion a np:Assertion .
  
  dgn-np:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_provenance a np:Provenance .
  
  dgn-np:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_assertion {
  miriam-gene:5827 a ncit:C16612 .
  
  lld:C0270922 a ncit:C7057 .
  
  dgn-gda:DGN675dbcd1900c40a1f51059d36a9d91cf sio:SIO_000628 miriam-gene:5827, lld:C0270922;
    a sio:SIO_001121 .
}

dgn-np:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_provenance {
  dgn-np:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_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-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:NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:35+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" .
}