@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg> .
@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/v3.0.0/void/> .
dgn-np:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_head {
  this: np:hasAssertion dgn-np:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_assertion ;
    np:hasProvenance dgn-np:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_provenance ;
    np:hasPublicationInfo dgn-np:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_assertion a np:Assertion .
  dgn-np:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_provenance a np:Provenance .
  dgn-np:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_assertion {
  miriam-gene:54332 a ncit:C16612 .
  lld:C0031117 a ncit:C7057 .
  dgn-gda:DGN17a51792244167f3f560d811b0b053a4 sio:SIO_000628 miriam-gene:54332 , lld:C0031117 ;
    a sio:SIO_001121 .
}
dgn-np:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_provenance {
  dgn-np:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_assertion dcterms:description "[We examine the relationship between the genotype and the phenotype in the various forms of CMT disease related to GDAP1 mutations, and discuss the pathophysiological hypotheses that link peripheral neuropathies to mitochondrial dysfunction and GDAP1 mutations.]. 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:20849849 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP910560.RAMDlXw4lefAZpvJcrz9sRfWT4ASgjsWydRkUOrIT4NSg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:55+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}