@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ> .
@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:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_head {
  this: np:hasAssertion dgn-np:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_assertion;
    np:hasProvenance dgn-np:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_provenance;
    np:hasPublicationInfo dgn-np:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_assertion a np:Assertion .
  
  dgn-np:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_provenance a np:Provenance .
  
  dgn-np:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_assertion {
  miriam-gene:613 a ncit:C16612 .
  
  lld:C0023473 a ncit:C7057 .
  
  dgn-gda:DGNc63210a9c0ddd0505235d503c4447c92 sio:SIO_000628 miriam-gene:613, lld:C0023473;
    a sio:SIO_001121 .
}

dgn-np:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_provenance {
  dgn-np:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_assertion dcterms:description
      "[Our results indicate that CML is a component of the NHIs of familial ALS patients with SOD1 mutation, and suggest that the CML formation may be mediated by protein glycoxidation or lipid peroxidation in the presence of oxidative stress from mutant SOD1, in association with motor neuron 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:10090670;
    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:NP162485.RAJuRLjASc3TqfA13X7yV9gMam6XDxZiW0zI4L6DOckbQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:28+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" .
}