@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP231967.RAhQsYndLUTrYELM2jJHMFxRSt1WUDKOLRzjbVsIJfcZg> .
@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:NP231967.RAhQsYndLUTrYELM2jJHMFxRSt1WUDKOLRzjbVsIJfcZg130_head {
  this: np:hasAssertion dgn-np:NP231967.RAhQsYndLUTrYELM2jJHMFxRSt1WUDKOLRzjbVsIJfcZg130_assertion;
    np:hasProvenance dgn-np:NP231967.RAhQsYndLUTrYELM2jJHMFxRSt1WUDKOLRzjbVsIJfcZg130_provenance;
    np:hasPublicationInfo dgn-np:NP231967.RAhQsYndLUTrYELM2jJHMFxRSt1WUDKOLRzjbVsIJfcZg130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP231967.RAhQsYndLUTrYELM2jJHMFxRSt1WUDKOLRzjbVsIJfcZg130_publicationInfo a
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dgn-np:NP231967.RAhQsYndLUTrYELM2jJHMFxRSt1WUDKOLRzjbVsIJfcZg130_assertion {
  miriam-gene:6683 a ncit:C16612 .
  
  lld:C0034152 a ncit:C7057 .
  
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dgn-np:NP231967.RAhQsYndLUTrYELM2jJHMFxRSt1WUDKOLRzjbVsIJfcZg130_provenance {
  dgn-np:NP231967.RAhQsYndLUTrYELM2jJHMFxRSt1WUDKOLRzjbVsIJfcZg130_assertion dcterms:description
      "[The motor-evoked potentials and the cortical excitability by transcranial magnetic stimulation (TMS) were studied in a family with chromosome 2p linked (due to mutations in spastin) and in a family with chromosome 16q linked (due to mutations in paraplegin) hereditary spastic paraparesis (HSP), in order to evaluate the utility of these techniques in identifying the subgroups of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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  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 .
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dgn-np:NP231967.RAhQsYndLUTrYELM2jJHMFxRSt1WUDKOLRzjbVsIJfcZg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    prv:usedData dgn-void:disgenetrdf;
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