@prefix dc: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc> .
@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 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:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_head {
  this: np:hasAssertion dgn-np:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_assertion;
    np:hasProvenance dgn-np:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_provenance;
    np:hasPublicationInfo dgn-np:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_assertion a np:Assertion .
  
  dgn-np:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_provenance a np:Provenance .
  
  dgn-np:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_assertion {
  miriam-gene:10743 a ncit:C16612 .
  
  lld:C0795864 a ncit:C7057 .
  
  dgn-gda:DGN214a95f010ad358f40d695d5b3a310da sio:SIO_000628 miriam-gene:10743, lld:C0795864;
    a sio:SIO_001121 .
}

dgn-np:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_provenance {
  dgn-np:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_assertion dc:description
      "[These results suggest that SMS needs to be considered in the differential diagnosis of autism spectrum disorders but also that therapeutic interventions for autism are likely to benefit individuals with SMS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:20981775;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP28126.RAD2QeLsiUREaJKmOdiq7YT0JjaE5bh2r1CAIzEs8BLWc130_publicationInfo {
  this: dc:created "2014-10-02T12:32:12+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}