@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY> .
@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:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_head {
  this: np:hasAssertion dgn-np:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_assertion;
    np:hasProvenance dgn-np:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_provenance;
    np:hasPublicationInfo dgn-np:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_assertion a np:Assertion .
  
  dgn-np:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_provenance a np:Provenance .
  
  dgn-np:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_assertion {
  miriam-gene:4359 a ncit:C16612 .
  
  lld:C0270911 a ncit:C7057 .
  
  dgn-gda:DGNbbdf6925dd7dd0edc0b33dd0a2563e81 sio:SIO_000628 miriam-gene:4359, lld:C0270911;
    a sio:SIO_001121 .
}

dgn-np:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_provenance {
  dgn-np:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_assertion dcterms:description
      "[While mutation in the gene encoding the major myelin protein, P0 has been associated with CMT1B, CMT1A and HNPP have been shown to be associated with reciprocal recombination events leading either to a large submicroscopic duplication in CMT1A, or the corresponding DNA deletion 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:7515304;
    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:NP609764.RAk2JinZQIuZJO4IdLyDkc8dEXKyxmhjVQQOOzPvbOWIY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:06+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" .
}