@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4> .
@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:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_head {
  this: np:hasAssertion dgn-np:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_assertion;
    np:hasProvenance dgn-np:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_provenance;
    np:hasPublicationInfo dgn-np:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_assertion a np:Assertion .
  
  dgn-np:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_provenance a np:Provenance .
  
  dgn-np:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_assertion {
  miriam-gene:8991 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGNf95e2249c28f8e8f35541e01a75b26d6 sio:SIO_000628 miriam-gene:8991, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_provenance {
  dgn-np:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_assertion dcterms:description
      "[One of four haplotype-tagging SNPs and two different two-marker haplotypes showed nominally significant evidence for association with schizophrenia under an additive model, suggesting that genetic variation in SELENBP1 may influence risk for the disorder, while this significance did not remain when other inheritance models were considered.]. 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:19596560;
    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:NP719587.RAhOId254a16fb48pjxHVvRHH4ktfdXN9KMcngn7byAf4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:17+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" .
}