@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms> .
@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:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_head {
  this: np:hasAssertion dgn-np:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_assertion;
    np:hasProvenance dgn-np:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_provenance;
    np:hasPublicationInfo dgn-np:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_assertion a np:Assertion .
  
  dgn-np:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_provenance a np:Provenance .
  
  dgn-np:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_assertion {
  miriam-gene:6647 a ncit:C16612 .
  
  lld:C1839259 a ncit:C7057 .
  
  dgn-gda:DGN605a9dc64ad9f4d32db738989b2c8035 sio:SIO_000628 miriam-gene:6647, lld:C1839259;
    a sio:SIO_001121 .
}

dgn-np:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_provenance {
  dgn-np:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_assertion dcterms:description
      "[Granular inclusions were also found in carriers of SOD1 mutations and in spinobulbar muscular atrophy (SBMA) patients and they were the major type of inclusion detected in ALS patients homozygous for the wild type-like D90A mutation.]. 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:20644736;
    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:NP811874.RAoWhUKP31-_-O3T7PSq_-KHI1i2bcYFKU9Rd_wuuZ_ms130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:18+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" .
}