@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M> .
@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:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_head {
  this: np:hasAssertion dgn-np:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_assertion;
    np:hasProvenance dgn-np:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_provenance;
    np:hasPublicationInfo dgn-np:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_assertion a np:Assertion .
  
  dgn-np:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_provenance a np:Provenance .
  
  dgn-np:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_assertion {
  miriam-gene:1639 a ncit:C16612 .
  
  lld:C0085084 a ncit:C7057 .
  
  dgn-gda:DGN03dcd4a8bfcb4d28c57bc39d25e06fdc sio:SIO_000628 miriam-gene:1639, lld:C0085084;
    a sio:SIO_001121 .
}

dgn-np:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_provenance {
  dgn-np:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_assertion dcterms:description
      "[Neuronal expression of mutant, but not wild type, dynactin p150(Glued) causes motor neuron disease in these animals that are characterized by defects in vesicular transport in cell bodies of motor neurons, axonal swelling and axo-terminal degeneration.]. 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:18305234;
    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:NP496231.RABIZvt26CrCOSrTM6B4g6vc5UWA3z5Mct9q3Y9SYFd9M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:56+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" .
}