@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM> .
@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:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_head {
  this: np:hasAssertion dgn-np:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_assertion;
    np:hasProvenance dgn-np:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_provenance;
    np:hasPublicationInfo dgn-np:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_assertion a np:Assertion .
  
  dgn-np:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_provenance a np:Provenance .
  
  dgn-np:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_assertion {
  miriam-gene:2521 a ncit:C16612 .
  
  lld:C0338451 a ncit:C7057 .
  
  dgn-gda:DGN052dd3b24999fba0c416c774687e1cce sio:SIO_000628 miriam-gene:2521, lld:C0338451;
    a sio:SIO_001121 .
}

dgn-np:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_provenance {
  dgn-np:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_assertion dcterms:description
      "[In particular, the progress in the molecular neuropathology with the discovery of pathogenic mutations in TAR DNA binding protein (TARDBP), fused in sarcoma (FUS), ubiquilin2 (UBQLN2) and most recently C9ORF72 (abbreviation for the open reading frame 72 on chromosome 9) has further substantiated the - clinically temporarily forgotten - relation of classic ALS to frontotemporal degeneration (FTD).]. 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:22918486;
    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:NP431291.RAkzpoAS9WcKJNsXLrN150dhf_kskZx61i8WDfgDNerpM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:15+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" .
}