@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8> .
@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:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_head {
  this: np:hasAssertion dgn-np:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_assertion;
    np:hasProvenance dgn-np:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_provenance;
    np:hasPublicationInfo dgn-np:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_assertion a np:Assertion .
  
  dgn-np:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_provenance a np:Provenance .
  
  dgn-np:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_assertion {
  miriam-gene:2332 a ncit:C16612 .
  
  lld:C0175702 a ncit:C7057 .
  
  dgn-gda:DGNd2c52ec121c6b93005bbe717e10fa277 sio:SIO_000628 miriam-gene:2332, lld:C0175702;
    a sio:SIO_001121 .
}

dgn-np:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_provenance {
  dgn-np:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_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:NP213123.RATp5-oWVaaQLo7gg9XTfl_k98T159EU_vxNntTL5DAe8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+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" .
}