@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo> .
@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:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_head {
  this: np:hasAssertion dgn-np:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_assertion;
    np:hasProvenance dgn-np:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_provenance;
    np:hasPublicationInfo dgn-np:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_assertion a np:Assertion .
  
  dgn-np:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_provenance a np:Provenance .
  
  dgn-np:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_assertion {
  miriam-gene:5293 a ncit:C16612 .
  
  lld:C0016667 a ncit:C7057 .
  
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dgn-np:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_provenance {
  dgn-np:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_assertion dcterms:description
      "[Our work suggests that dys-regulated protein synthesis and PI3K activity in patient cells might be suitable biomarkers to quantify the efficacy of drugs to ameliorate molecular mechanisms underlying FXS, and could be used for drug screens to refine treatment strategies for individual patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP430162.RAMadW8pzK_Hpj6wtd9BUDils0VhLwiUCgbbnc2GgdHKo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:15+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" .
}