@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ> .
@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:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_head {
   this: np:hasAssertion dgn-np:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_assertion ;
    np:hasProvenance dgn-np:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_assertion a np:Assertion .
  dgn-np:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_provenance a np:Provenance .
  dgn-np:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_assertion {
   miriam-gene:6683 a ncit:C16612 .
  lld:C0034152 a ncit:C7057 .
  dgn-gda:DGN3b884614173c30486002044d6bb7cf9a sio:SIO_000628 miriam-gene:6683 , lld:C0034152 ;
    a sio:SIO_001121 .
}
dgn-np:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_provenance {
   dgn-np:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_assertion dcterms:description "[Genotyping the two sets of MS patients and controls could not provide any evidence to suggest that genes involved in the pathogenesis of HSP (Paraplegin, NIPA1, KIF5A, HSPD1, Atlastin, Spartin, Spastin, PLP1, L1CAM, Maspardin and BSCL2) play a role in susceptibility to, or modifying the course of, MS, although small effects of these genes cannot be ruled out.]. 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:NP176294.RAVl0_3mpWefnnrgTBqnD1iTVulPCYHfXYbya4ZA9znpQ130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:35+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" .
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}