@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk> .
@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:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_head {
  this: np:hasAssertion dgn-np:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_assertion ;
    np:hasProvenance dgn-np:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_provenance ;
    np:hasPublicationInfo dgn-np:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_assertion a np:Assertion .
  dgn-np:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_provenance a np:Provenance .
  dgn-np:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_assertion {
  miriam-gene:8444 a ncit:C16612 .
  lld:C1839839 a ncit:C7057 .
  dgn-gda:DGNfad6d9154aef2a5a1039ba8c007c41e2 sio:SIO_000628 miriam-gene:8444 , lld:C1839839 ;
    a sio:SIO_001121 .
}
dgn-np:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_provenance {
  dgn-np:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_assertion dcterms:description "[The purpose of the present study was to further test if expanded CAG repeats detected by the repeat expansion detection (RED) method in bipolar affective disorder (BPAD) are correlated with ERDA1 (17q21.3) and/or CTG18.1 (18q21.1) loci expansions, and changes of phenotype severity in successive generations (anticipation).]. 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:15211635 ;
    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:NP885159.RANiNMV9FjE4LaiLpJoieIzY3hp0dHy5S7PMYEOC0snFk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:00+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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