@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ> .
@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:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_head {
  this: np:hasAssertion dgn-np:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_assertion;
    np:hasProvenance dgn-np:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_provenance;
    np:hasPublicationInfo dgn-np:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_assertion a np:Assertion .
  
  dgn-np:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_provenance a np:Provenance .
  
  dgn-np:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_assertion {
  miriam-gene:6683 a ncit:C16612 .
  
  lld:C0011265 a ncit:C7057 .
  
  dgn-gda:DGN74faccb4898b43e0901dba050ce9b3a6 sio:SIO_000628 miriam-gene:6683, lld:C0011265;
    a sio:SIO_001121 .
}

dgn-np:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_provenance {
  dgn-np:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_assertion dcterms:description
      "[In addition, the seven different loci so far reported to be associated with autosomal dominant pure forms of spastic paraplegia have been tested and excluded by linkage analysis and haplotype reconstruction, including SPG4 on chromosome 2p22-p21, where a familial form of spastic paraplegia associated with dementia and epilepsy has been mapped.]. 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:12567407;
    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:NP205618.RAbr54hLWeaSWckRY8nQDQ1mU9ydaspFJvUj5DOLKxUKQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:53+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" .
}