@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc> .
@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:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_head {
  this: np:hasAssertion dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_assertion;
    np:hasProvenance dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_provenance;
    np:hasPublicationInfo dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_assertion a np:Assertion .
  
  dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_provenance a np:Provenance .
  
  dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_assertion {
  miriam-gene:1917 a ncit:C16612 .
  
  lld:C0235394 a ncit:C7057 .
  
  dgn-gda:DGN0ebc938c064d635e38c2caf0806e0b98 sio:SIO_000628 miriam-gene:1917, lld:C0235394;
    a sio:SIO_001121 .
}

dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_provenance {
  dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_assertion dcterms:description
      "[We conclude that spontaneous failure of eEF1A2 expression in the wasted mutant first triggers gliosis in spinal cord and retraction of motor nerve terminals in muscle, and then motor neuron pathology and death.]. 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:15835265;
    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:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:44+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" .
}