@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE> .
@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:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_head {
  this: np:hasAssertion dgn-np:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_assertion ;
    np:hasProvenance dgn-np:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_provenance ;
    np:hasPublicationInfo dgn-np:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_assertion a np:Assertion .
  dgn-np:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_provenance a np:Provenance .
  dgn-np:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_assertion {
  miriam-gene:7472 a ncit:C16612 .
  lld:C0004352 a ncit:C7057 .
  dgn-gda:DGN16844ec70c445f4e8947aa8cc85e9baf sio:SIO_000628 miriam-gene:7472 , lld:C0004352 ;
    a sio:SIO_001121 .
}
dgn-np:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_provenance {
  dgn-np:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_assertion dcterms:description "[We genotyped all four WNT2 polymorphisms and a polymorphic trinucleotide repeat in the 5' UTR of RELN in 107 families with multiple autistic children, and evaluated evidence for association between these variants and autism by the transmission disequilibrium test (TDT).]. 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:15048648 ;
    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:NP840493.RA9_EubrLF4LNZsQK3hEFeIPtx-Eh6RrzThJZmkZkQmQE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:34+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" .
}