@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA> .
@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:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_head {
   this: np:hasAssertion dgn-np:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_assertion ;
    np:hasProvenance dgn-np:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_provenance ;
    np:hasPublicationInfo dgn-np:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_assertion a np:Assertion .
  dgn-np:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_provenance a np:Provenance .
  dgn-np:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_assertion {
   miriam-gene:4359 a ncit:C16612 .
  lld:C0393818 a ncit:C7057 .
  dgn-gda:DGN7c6d58d3771bbaaf44f8badd98a4893e sio:SIO_000628 miriam-gene:4359 , lld:C0393818 ;
    a sio:SIO_001121 .
}
dgn-np:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_provenance {
   dgn-np:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_assertion dcterms:description "[The spectrum of Charcot-Marie-Tooth (CMT) phenotypes segregating with mutations in the Myelin Protein Zero (MPZ) gene is wide and ranges from congenital hypomyelinating neuropathy (CHN) through demyelinating form of CMT to the axonal type of CMT disease.]. 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:15261887 ;
    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:NP452558.RAfvkkO1fcJjmodsE1DVI0LeSuiCN391fq6lQXRvY9HFA130_publicationInfo {
   this: dcterms:created "2016-05-13T12:45:10+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" .
}