@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ> .
@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:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_head {
  this: np:hasAssertion dgn-np:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_assertion;
    np:hasProvenance dgn-np:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_provenance;
    np:hasPublicationInfo dgn-np:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_assertion a np:Assertion .
  
  dgn-np:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_provenance a np:Provenance .
  
  dgn-np:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_assertion {
  miriam-gene:1038 a ncit:C16612 .
  
  lld:C0262404 a ncit:C7057 .
  
  dgn-gda:DGN75dec33d23d336a9995b08503db51339 sio:SIO_000628 miriam-gene:1038, lld:C0262404;
    a sio:SIO_001121 .
}

dgn-np:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_provenance {
  dgn-np:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_assertion dcterms:description
      "[This study narrows down the localization of the gene coding for the cerebellar degeneration-related protein (CDR 34) to the upper boundary of the FRAXA and reports the finding of two common RFLPs respectively identified at an RsaI site flanking the 3' end of the gene and at a Hincll site flanking its 5' end.]. 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:1708201;
    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:NP908802.RAjk8UShwSrduf_P4XpPqP_451ZYc11vo_ffLIuDM4XNQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:18+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" .
}