@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg> .
@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:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_head {
  this: np:hasAssertion dgn-np:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_assertion;
    np:hasProvenance dgn-np:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_provenance;
    np:hasPublicationInfo dgn-np:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_assertion a np:Assertion .
  
  dgn-np:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_provenance a np:Provenance .
  
  dgn-np:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_assertion {
  miriam-gene:7298 a ncit:C16612 .
  
  lld:C0037771 a ncit:C7057 .
  
  dgn-gda:DGNc6c9737740fcfad59e25afd6b36582dc sio:SIO_000628 miriam-gene:7298, lld:C0037771;
    a sio:SIO_001121 .
}

dgn-np:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_provenance {
  dgn-np:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_assertion dcterms:description
      "[The aim of our study was to evaluate Motor Evoked Potentials (MEPs) and cortical excitability, using Transcranial Magnetic Stimulation (TMS) as well as short latency Somatosensory Evoked Potentials (SEPs) in Autosomal Dominant Hereditary Spastic Paraparesis (ADHSP) patients.]. 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:17720546;
    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:NP605545.RAbI9hZkzyJ0q0lVrW3ZkvYyflu03PCxRdbJVfd3AF-gg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:03+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" .
}