@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g> .
@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:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_head {
  this: np:hasAssertion dgn-np:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_assertion;
    np:hasProvenance dgn-np:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_provenance;
    np:hasPublicationInfo dgn-np:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_assertion a np:Assertion .
  
  dgn-np:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_provenance a np:Provenance .
  
  dgn-np:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_assertion {
  miriam-gene:2477 a ncit:C16612 .
  
  lld:C0027831 a ncit:C7057 .
  
  dgn-gda:DGNeff3ba6367680781a72b44765b5de1f6 sio:SIO_000628 miriam-gene:2477, lld:C0027831;
    a sio:SIO_001121 .
}

dgn-np:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_provenance {
  dgn-np:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_assertion dcterms:description
      "[In this study, we examine longitudinal changes in IQ and DQ in children with neurofibromatosis type 1 (NF1) and Williams-Beuren Syndrome (WBS) by examining differences in composite IQ and DQ scores between the first test (T1) and retest (T2), and compare their developmental trajectory to children with the FMR1 mutation.]. 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:20503326;
    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:NP572080.RAiyXDC2viJiOLO0YuQSs2vXXv6SyKBv-TC2o0Dgp7P_g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:45+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" .
}