@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0> .
@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:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_head {
  this: np:hasAssertion dgn-np:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_assertion;
    np:hasProvenance dgn-np:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_provenance;
    np:hasPublicationInfo dgn-np:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_assertion a np:Assertion .
  
  dgn-np:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_provenance a np:Provenance .
  
  dgn-np:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_assertion {
  miriam-gene:57760 a ncit:C16612 .
  
  lld:C1858712 a ncit:C7057 .
  
  dgn-gda:DGNf09d8d55082eda504b545ec0b5415aae sio:SIO_000628 miriam-gene:57760, lld:C1858712;
    a sio:SIO_001121 .
}

dgn-np:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_provenance {
  dgn-np:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_assertion dcterms:description
      "[More than 20 HSP loci and 10 spastic paraplegia genes (SPG) have been identified to date, including the genes responsible for the two most frequent forms of autosomal dominant spastic paraplegia (AD-HSP), encoding spastin (SPG4) and atlastin (SPG3A), respectively.]. 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:15517445;
    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:NP829637.RAuVXC7jokLX8z-iZXOMb4-xYNoIXFS02uorbrS_oGPF0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:27+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: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" .
}