@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk> .
@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:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_head {
  this: np:hasAssertion dgn-np:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_assertion ;
    np:hasProvenance dgn-np:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_provenance ;
    np:hasPublicationInfo dgn-np:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_assertion a np:Assertion .
  dgn-np:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_provenance a np:Provenance .
  dgn-np:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_assertion {
  miriam-gene:5376 a ncit:C16612 .
  lld:C0152025 a ncit:C7057 .
  dgn-gda:DGNe9e6e7878faa0f5676df5b06b68651cb sio:SIO_000628 miriam-gene:5376 , lld:C0152025 ;
    a sio:SIO_001121 .
}
dgn-np:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_provenance {
  dgn-np:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_assertion dcterms:description "[The distribution and severity of the background electrophysiologic abnormalities are closely related to the topography of common entrapment or compression sites, which suggests the possible pathogenetic role of subclinical pressure injury at these sites in the development of the distinct background polyneuropathy in HNPP.]. 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:14616306 ;
    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:NP471790.RAd2wHT_TstftcFvxp_ftSz7yNGi9sX8iFLgDvoujE2Rk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:43+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" .
}