@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE> .
@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:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_head {
  this: np:hasAssertion dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_assertion;
    np:hasProvenance dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_provenance;
    np:hasPublicationInfo dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_assertion a np:Assertion .
  
  dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_provenance a np:Provenance .
  
  dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_assertion {
  miriam-gene:2477 a ncit:C16612 .
  
  lld:C0242422 a ncit:C7057 .
  
  dgn-gda:DGN9ff669e943a2210d6deaf65208bb5396 sio:SIO_000628 miriam-gene:2477, lld:C0242422;
    a sio:SIO_001121 .
}

dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_provenance {
  dgn-np:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_assertion dcterms:description
      "[Special emphasis has been placed on the possibility that the modest elevation of 'toxic' FMR1 mRNA in the carriers of grey zone alleles may present an additional risk for some neurodegenerative diseases, such as those associated with parkinsonism, by synergizing with either other susceptibility genes or environmental poisons.]. 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:23560306;
    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:NP587607.RAJB5t8qzrUt9KruxZ5pAK-An-uVxX050V6ISOMJARgrE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:53+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" .
}