@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24> .
@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:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_head {
  this: np:hasAssertion dgn-np:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_assertion;
    np:hasProvenance dgn-np:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_provenance;
    np:hasPublicationInfo dgn-np:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_assertion a np:Assertion .
  
  dgn-np:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_provenance a np:Provenance .
  
  dgn-np:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_assertion {
  miriam-gene:9587 a ncit:C16612 .
  
  lld:C0011195 a ncit:C7057 .
  
  dgn-gda:DGN16e8b04d3060b8888f8bb0293019c484 sio:SIO_000628 miriam-gene:9587, lld:C0011195;
    a sio:SIO_001121 .
}

dgn-np:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_provenance {
  dgn-np:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_assertion dcterms:description
      "[Point mutations in the coding region of the myelin genes, peripheral myelin protein 22 (PMP22), myelin protein zero (MPZ) or connexin 32 (Cx32) have been reported in CMT patients, including CMT type 1 (CMT1), CMT type 2 (CMT2) and Déjérine-Sottas neuropathy (DS) patients, and only in the coding region of PMP22 in HNPP families lacking a deletion.]. 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:9187667;
    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:NP863145.RAoj34BCbRyQx06IUYGdpA8BLSt0fRjwu4YeUqs_a6w24130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:47+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" .
}