@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_head {
  this: np:hasAssertion dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_assertion;
    np:hasProvenance dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_provenance;
    np:hasPublicationInfo dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_assertion a np:Assertion .
  
  dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_provenance a np:Provenance .
  
  dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_assertion {
  miriam-gene:6647 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGNfff7d35e660088540f6330b83a315a13 sio:SIO_000628 miriam-gene:6647, lld:C0002736;
    a sio:SIO_001121 .
}

dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_provenance {
  dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_assertion dcterms:description
      "[Focusing on amyotrophic lateral sclerosis (ALS), especially disease caused by dominant mutations in Cu/Zn superoxide dismutase (SOD1), we review here the evidence that it is the convergence of damage developed within multiple cell types, including within neighboring nonneuronal supporting cells, which is crucial to neuronal dysfunction.]. 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:19951898;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:38+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}