@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY> .
@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:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_head {
  this: np:hasAssertion dgn-np:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_assertion ;
    np:hasProvenance dgn-np:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_provenance ;
    np:hasPublicationInfo dgn-np:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_assertion a np:Assertion .
  dgn-np:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_provenance a np:Provenance .
  dgn-np:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_assertion {
  miriam-gene:2739 a ncit:C16612 .
  lld:C0004352 a ncit:C7057 .
  dgn-gda:DGN0553a62812c43a228df95b0e8590a1e6 sio:SIO_000628 miriam-gene:2739 , lld:C0004352 ;
    a sio:SIO_001121 .
}
dgn-np:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_provenance {
  dgn-np:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_assertion dcterms:description "[To investigate whether common variants in GLO1 predispose to autism in the Finnish population, we have genotyped six polymorphisms in GLO1 in families with more than 230 individuals affected with ASDs and carried out both linkage and association analyses.]. 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:17722011 ;
    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:NP363534.RAlIkM1TiYBYV26UQ2dXAkZIRCHw52eobMu5rnL2MF4aY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:33+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" .
}