@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0> .
@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:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_head {
  this: np:hasAssertion dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_assertion;
    np:hasProvenance dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_provenance;
    np:hasPublicationInfo dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_assertion a np:Assertion .
  
  dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_provenance a np:Provenance .
  
  dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_assertion {
  miriam-gene:23025 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGN2722972debd72201e0d71ed78e8a57c6 sio:SIO_000628 miriam-gene:23025, lld:C0002736;
    a sio:SIO_001122 .
}

dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_provenance {
  dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_assertion dcterms:description
      "[The common variant rs12608932, located within an intron of UNC13A gene on chromosome 19p13.3, has been suggested to influence susceptibility to amyotrophic lateral sclerosis (ALS), as well as survival, in patients of north European descent.]. 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:22921269;
    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:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:27+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" .
}