@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA> .
@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:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_head {
  this: np:hasAssertion dgn-np:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_assertion;
    np:hasProvenance dgn-np:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_provenance;
    np:hasPublicationInfo dgn-np:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_assertion a np:Assertion .
  
  dgn-np:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_provenance a np:Provenance .
  
  dgn-np:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_assertion {
  miriam-gene:7190 a ncit:C16612 .
  
  lld:C0034152 a ncit:C7057 .
  
  dgn-gda:DGN6ef7a8c843c6db5dc79fcfe154fc7bac sio:SIO_000628 miriam-gene:7190, lld:C0034152;
    a sio:SIO_001121 .
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dgn-np:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_provenance {
  dgn-np:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_assertion dcterms:description
      "[The clinical similarities between Hereditary Spastic Paraplegia (HSP) and progressive MS, along with their analogous profiles of axonal loss in the long tracts, make the genes known to cause HSP biologically relevant candidates for the study of clinical outcome in MS. A cohort of sporadic MS cases and a set of unaffected controls were used to determine the role of HSP genes on MS susceptibility and disease severity.]. 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:17420921;
    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:NP683928.RAooB2bAApH7kBou7jqFvAtTRqXkExThTP9QF_87iKZCA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}