@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM> .
@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/v4.0.0/void/> .

dgn-np:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_head {
  this: np:hasAssertion dgn-np:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_assertion;
    np:hasProvenance dgn-np:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_provenance;
    np:hasPublicationInfo dgn-np:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_assertion a np:Assertion .
  
  dgn-np:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_provenance a np:Provenance .
  
  dgn-np:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_assertion {
  miriam-gene:6647 a ncit:C16612 .
  
  lld:C0085084 a ncit:C7057 .
  
  dgn-gda:DGN428f45534234cb55138e453de2554f6a sio:SIO_000628 miriam-gene:6647, lld:C0085084;
    a sio:SIO_001122 .
}

dgn-np:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_provenance {
  dgn-np:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_assertion dcterms:description
      "[Since the mechanism whereby mutations in SOD1 lead to MND remains enigmatic, we asked whether NF inclusions in motor neurons compromise axonal transport during the onset and progression of MND in a line of mice that contained approximately 30% fewer copies of the transgene than the original G93A (Gurney et al., 1994).]. 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:9382875;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1384589.RAACKy98Rruy8_ZFHEJzN6cStcK2kdnksDH6t75xdDkkM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:14+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}