@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk> .
@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:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_head {
  this: np:hasAssertion dgn-np:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_assertion ;
    np:hasProvenance dgn-np:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_provenance ;
    np:hasPublicationInfo dgn-np:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_assertion a np:Assertion .
  dgn-np:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_provenance a np:Provenance .
  dgn-np:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_assertion {
  miriam-gene:5827 a ncit:C16612 .
  lld:C0393814 a ncit:C7057 .
  dgn-gda:DGNe2502f8429f26c5350d810a959a1cb60 sio:SIO_000628 miriam-gene:5827 , lld:C0393814 ;
    a sio:SIO_001121 .
}
dgn-np:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_provenance {
  dgn-np:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_assertion dcterms:description "[We retrospectively analyzed paraffin-embedded sural nerve biopsy specimens from cases suspected of having dominantly inherited motor and sensory neuropathy (HMSN) or hereditary neuropathy with liability to pressure palsy (HNPP), with respect to their proportional DNA content at chromosome 17p11.2-12, encompassing the PMP-22 gene, using polymerase chain reaction (PCR).]. 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:9678509 ;
    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:NP709871.RAEzR4wJytTTXVhh6vRqZQJfMZiGxM-fkToYW12HuvTqk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:11+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" .
}