@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc> .
@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:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_head {
   this: np:hasAssertion dgn-np:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_assertion ;
    np:hasProvenance dgn-np:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_provenance ;
    np:hasPublicationInfo dgn-np:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_assertion a np:Assertion .
  dgn-np:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_provenance a np:Provenance .
  dgn-np:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_assertion {
   miriam-gene:7143 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
  dgn-gda:DGN57f8b484b5f891dc061cc0cb973adfb0 sio:SIO_000628 miriam-gene:7143 , lld:C0036341 ;
    a sio:SIO_001121 .
}
dgn-np:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_provenance {
   dgn-np:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_assertion dcterms:description "[Ten genes of importance for HNK-1 biosynthesis (B3GAT1, B3GAT2, and CHST10) or for the formation of perineuronal nets (TNR, BCAN, NCAN, HAPLN1, HAPLN2, HAPLN3, and HAPLN4) were investigated for potential involvement in schizophrenia (SCZ) susceptibility, by genotyping 104 tagSNPs in the Scandinavian Collaboration on Psychiatric Etiology sample (849 cases; 1602 control subjects).]. 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:20950796 ;
    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:NP871556.RAREqZVlYbc40mXeKzovbXPInZYjCZB8SOj8D5ivKlNPc130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:53+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> ;
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