@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA> .
@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:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_head {
  this: np:hasAssertion dgn-np:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_assertion ;
    np:hasProvenance dgn-np:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_provenance ;
    np:hasPublicationInfo dgn-np:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_assertion a np:Assertion .
  dgn-np:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_provenance a np:Provenance .
  dgn-np:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_assertion {
  miriam-gene:6647 a ncit:C16612 .
  lld:C0001614 a ncit:C7057 .
  dgn-gda:DGN6069a8def986669f0a3f0f094285e6b5 sio:SIO_000628 miriam-gene:6647 , lld:C0001614 ;
    a sio:SIO_001121 .
}
dgn-np:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_provenance {
  dgn-np:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_assertion dcterms:description "[We stimulated the motor cortex of ten patients homozygous for the D90A SOD1 mutation, using transcranial magnetic stimulation (TMS), and recorded the response evoked in the right first dorsal interosseous muscle when the muscle was at rest and when voluntarily active.]. 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:15170611 ;
    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:NP436771.RA51Xnr2bkFH-Cc6KWUxftXLqVYLHFn9cSJj_P5kCetAA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:18+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" .
}