@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY> .
@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:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_head {
  this: np:hasAssertion dgn-np:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_assertion;
    np:hasProvenance dgn-np:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_provenance;
    np:hasPublicationInfo dgn-np:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_assertion a np:Assertion .
  
  dgn-np:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_provenance a np:Provenance .
  
  dgn-np:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_assertion {
  miriam-gene:3925 a ncit:C16612 .
  
  lld:C0026846 a ncit:C7057 .
  
  dgn-gda:DGN863a37aa77d8700cd5e848efbcf21cc0 sio:SIO_000628 miriam-gene:3925, lld:C0026846;
    a sio:SIO_001121 .
}

dgn-np:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_provenance {
  dgn-np:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_assertion dcterms:description
      "[Among diseases involving LMN degeneration, spinal muscular atrophy (SMA) and spinal bulbar muscular atrophy (Kennedy's disease, SBMA) are pure genetic diseases linked to loss of the SMN gene (SMA) or expansion of a polyglutamine tract in the androgen receptor gene (SBMA) while amyotrophic lateral sclerosis (ALS) can either be of genetic origin or occur sporadically.]. 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:20840067;
    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:NP838964.RAGtV4rPkKcLDDAonVIJV148_3DEB0RSO4j0I56ke1wrY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:05+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" .
}