@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk> .
@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:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_head {
  this: np:hasAssertion dgn-np:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_assertion ;
    np:hasProvenance dgn-np:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_provenance ;
    np:hasPublicationInfo dgn-np:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_assertion a np:Assertion .
  dgn-np:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_provenance a np:Provenance .
  dgn-np:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_assertion {
  miriam-gene:4650 a ncit:C16612 .
  lld:C0004364 a ncit:C7057 .
  dgn-gda:DGN782961394f2dbe3140e4a83f2a9ddf9d sio:SIO_000628 miriam-gene:4650 , lld:C0004364 ;
    a sio:SIO_001121 .
}
dgn-np:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_provenance {
  dgn-np:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_assertion dcterms:description "[There has long been discussion on the correlation between schizophrenia and autoimmune diseases (especially celiac disease), which makes the recently discovered celiac disease risk factor, MYO9B, an attractive functional and positional candidate gene for schizophrenia.]. 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:17948900 ;
    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:NP898162.RAs6d_t586phwhhnfH3l_sW3TOsS6btLtptxbl5YEE4Fk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:12+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" .
}