@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc> .
@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:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_head {
  this: np:hasAssertion dgn-np:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_assertion;
    np:hasProvenance dgn-np:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_provenance;
    np:hasPublicationInfo dgn-np:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_assertion a np:Assertion .
  
  dgn-np:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_provenance a np:Provenance .
  
  dgn-np:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_assertion {
  miriam-gene:5827 a ncit:C16612 .
  
  lld:C0027888 a ncit:C7057 .
  
  dgn-gda:DGNb0d64263bb198112d32397869c535c7b sio:SIO_000628 miriam-gene:5827, lld:C0027888;
    a sio:SIO_001121 .
}

dgn-np:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_provenance {
  dgn-np:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_assertion dcterms:description
      "[A moderate increase in the number of PMP22 genes led to hypomyelination comparable to CMT1A, whereas high copy numbers of transgenic PMP22 resulted in phenotypes resembling more severe forms of hereditary motor and sensory neuropathies.]. 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:10586249;
    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:NP929245.RA9ptAOTj6Trufoohaafg2TPwXKY0y6M81spONxdAACdc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:30+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" .
}