@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A> .
@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:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_head {
   this: np:hasAssertion dgn-np:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_assertion ;
    np:hasProvenance dgn-np:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_provenance ;
    np:hasPublicationInfo dgn-np:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_assertion a np:Assertion .
  dgn-np:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_provenance a np:Provenance .
  dgn-np:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_assertion {
   miriam-gene:2332 a ncit:C16612 .
  lld:C0260653 a ncit:C7057 .
  dgn-gda:DGN6a0d3904593e6bd6a21cffd6deca1d2a sio:SIO_000628 miriam-gene:2332 , lld:C0260653 ;
    a sio:SIO_001121 .
}
dgn-np:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_provenance {
   dgn-np:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_assertion dcterms:description "[We conducted an in-home evaluation of 120 children (80 boys and 40 girls) with the fragile X full mutation and their unaffected siblings, including measurements of the FMR1 protein (FMRP), quality of the home environment, maternal and paternal psychopathology, effectiveness of educational and therapeutic services, and child behavior problems.]. 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:11694672 ;
    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:NP570337.RA5lNy8eylERcQifYTegzDhGb_zOtgYk2oQrBykPeR21A130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:44+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> ;
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}