@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg> .
@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:NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg130_head {
  this: np:hasAssertion dgn-np:NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg130_assertion ;
    np:hasProvenance dgn-np:NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg130_provenance ;
    np:hasPublicationInfo dgn-np:NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg130_provenance a np:Provenance .
  dgn-np:NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg130_assertion {
  miriam-gene:6513 a ncit:C16612 .
  lld:C0034152 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg130_provenance {
  dgn-np:NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg130_assertion dcterms:description "[We tested whether 1) progressive spastic paraparesis, in addition to PED, as described in DYT9, and 2) autosomal dominant forms of hereditary spastic paraparesis (HSP) without PED are caused by SLC2A1 defects.]. 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:21832227 ;
    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:NP895071.RAq1XmV044JLrBMuOM7H57UKalzM7m3KPeuzGEOpT3qRg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:10+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}