@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco> .
@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:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_head {
  this: np:hasAssertion dgn-np:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_assertion;
    np:hasProvenance dgn-np:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_provenance;
    np:hasPublicationInfo dgn-np:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_assertion a np:Assertion .
  
  dgn-np:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_provenance a np:Provenance .
  
  dgn-np:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0524851 a ncit:C7057 .
  
  dgn-gda:DGN6510f9dda22a0b795af16fb9cb1046ef sio:SIO_000628 miriam-gene:4397, lld:C0524851;
    a sio:SIO_001121 .
}

dgn-np:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_provenance {
  dgn-np:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_assertion dcterms:description
      "[Axon loss contributes to neurological symptoms in disorders as diverse as multiple sclerosis, stroke, traumatic brain and spinal cord injury, peripheral neuropathies and chronic neurodegenerative diseases, but it has been largely neglected in neuroprotective strategies.]. 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:12220882;
    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:NP480979.RA3ey16RZIaiUAPqMiM4RSY7-KrpSJwnXtBO7FuQh0Nco130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:48+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" .
}