@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8> .
@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:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_head {
  this: np:hasAssertion dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_assertion;
    np:hasProvenance dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_provenance;
    np:hasPublicationInfo dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_assertion a np:Assertion .
  
  dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_provenance a np:Provenance .
  
  dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_assertion {
  miriam-gene:6647 a ncit:C16612 .
  
  lld:C1883552 a ncit:C7057 .
  
  dgn-gda:DGNb75f77f158ec82f440a118be15e27282 sio:SIO_000628 miriam-gene:6647, lld:C1883552;
    a sio:SIO_001121 .
}

dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_provenance {
  dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_assertion dcterms:description
      "[Based on the temporal correlation of these impairments with the onset of motor weakness and the appearance of NF inclusions and vacuoles in vulnerable motor neurons, the latter lesions may be the proximal cause of motor neuron dysfunction and degeneration in the G93A mice and in FALS patients with SOD1 mutations.]. 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-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:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:10+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" .
}