@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM> .
@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:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_head {
  this: np:hasAssertion dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_assertion ;
    np:hasProvenance dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_provenance ;
    np:hasPublicationInfo dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_assertion a np:Assertion .
  dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_provenance a np:Provenance .
  dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_assertion {
  miriam-gene:613 a ncit:C16612 .
  lld:C1862939 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_provenance {
  dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_assertion dcterms:description "[To clarify the neuropathological significance of the deposition of N(epsilon)-carboxymethyl lysine (CML), an advanced glycation endproduct, in astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis (FALS), autopsy specimens from five members of two different families who had the superoxide dismutase 1 (SOD1) gene mutations were analysed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:50+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 ;
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}