@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0> .
@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:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_head {
  this: np:hasAssertion dgn-np:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_assertion ;
    np:hasProvenance dgn-np:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_provenance ;
    np:hasPublicationInfo dgn-np:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_assertion a np:Assertion .
  dgn-np:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_provenance a np:Provenance .
  dgn-np:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_assertion {
  miriam-gene:23095 a ncit:C16612 .
  lld:C0151786 a ncit:C7057 .
  dgn-gda:DGNc984dea028724f88b4c5bdc5e2853b6c sio:SIO_000628 miriam-gene:23095 , lld:C0151786 ;
    a sio:SIO_001121 .
}
dgn-np:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_provenance {
  dgn-np:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_assertion dcterms:description "[The clinical features of the CMT2A affecting the two families include similar levels of muscle weakness of the posterior and anterior tibial muscles, tendon reflexes preserved in upper extremities but reduced or absent in lower extremities, no enlargement of the peripheral nerves, and mild sensory disturbance in only 20% of affected individuals.]. 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:9409358 ;
    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:NP724796.RADaNsoronef8Se8rJk8l60Z2EfdakAfJZbWHB94hZAg0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:20+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
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}