@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M> .
@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/v3.0.0/void/> .

dgn-np:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_head {
  this: np:hasAssertion dgn-np:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_assertion;
    np:hasProvenance dgn-np:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_provenance;
    np:hasPublicationInfo dgn-np:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_assertion a np:Assertion .
  
  dgn-np:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_provenance a np:Provenance .
  
  dgn-np:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_assertion {
  miriam-gene:6647 a ncit:C16612 .
  
  lld:C1862939 a ncit:C7057 .
  
  dgn-gda:DGN0e86452bd47fb672836a71a4991975c1 sio:SIO_000628 miriam-gene:6647, lld:C1862939;
    a sio:SIO_001121 .
}

dgn-np:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_provenance {
  dgn-np:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_assertion dcterms:description
      "[The hypothesis that dissociation of the dimer, misfolding of the monomer and subsequent aggregation of mutant SOD1 leads to fALS has been gaining support as an explanation for how these disparate missense mutations cause the same disease.]. 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:23784844;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP706677.RAioxrfNypH6WM4fBmsrtVOoL3UU0hlrg1BuPwpacSI4M130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:46+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}