@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_head {
   this: np:hasAssertion dgn-np:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_assertion ;
    np:hasProvenance dgn-np:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_provenance ;
    np:hasPublicationInfo dgn-np:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_assertion a np:Assertion .
  dgn-np:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_provenance a np:Provenance .
  dgn-np:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_assertion {
   miriam-gene:8831 a ncit:C16612 .
  lld:C0018817 a ncit:C7057 .
  dgn-gda:DGN8761c895ae0286b6fe19094e39c226b7 sio:SIO_000628 miriam-gene:8831 , lld:C0018817 ;
    a sio:SIO_001121 .
}
dgn-np:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_provenance {
   dgn-np:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_assertion dcterms:description "[To further explore the involvement of SYNGAP1 in NSID, we sequenced its exons and intronic boundaries in 60 additional sporadic cases of NSID, including 30 patients with autism spectrum disorders (ASD) and 9 with epilepsy, and in 380 control individuals.]. 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:21237447 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP807038.RAkS_JlV14H88x2fw8dcJxob4j3iyE65PVssjOmkWMKTE130_publicationInfo {
   this: dcterms:created "2015-08-25T14:45:49+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}