@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_head {
  this: np:hasAssertion dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_assertion;
    np:hasProvenance dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_provenance;
    np:hasPublicationInfo dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_assertion a np:Assertion .
  
  dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_provenance a np:Provenance .
  
  dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_assertion {
  miriam-gene:2705 a ncit:C16612 .
  
  lld:C0393808 a ncit:C7057 .
  
  dgn-gda:DGN818030d80e60a46b4b353898f1507032 sio:SIO_000628 miriam-gene:2705, lld:C0393808;
    a sio:SIO_001121 .
}

dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_provenance {
  dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_assertion dcterms:description
      "[In addition, engineered mutants heterozygously or homozygously deficient in the myelin component P0 show the pathology of distinct CMT1B and DS patients, respectively, while Cx32 deficient mice develop pathological abnormalities similar to those of CMTX patients.]. 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:9418989;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:14+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}