@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU> .
@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:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_head {
  this: np:hasAssertion dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_assertion;
    np:hasProvenance dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_provenance;
    np:hasPublicationInfo dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_assertion a np:Assertion .
  
  dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_provenance a np:Provenance .
  
  dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_assertion {
  miriam-gene:3782 a ncit:C16612 .
  
  lld:C0349204 a ncit:C7057 .
  
  dgn-gda:DGNe5f5d6f52048a9c59e6cda7eb7767db8 sio:SIO_000628 miriam-gene:3782, lld:C0349204;
    a sio:SIO_001121 .
}

dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_provenance {
  dgn-np:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_assertion dcterms:description
      "[Our results support the hypothesis that a contribution of the KCNN3 gene to genetic susceptibility to major psychosis and their phenotypic polymorphism may be related to the difference of allele length rather than to the number of CAG repeats.]. 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:12960745;
    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:NP692889.RAR6UzRFEvRC9Tcc6PTIbKMKd7nNmeERCbGGbfnPCrglU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:01+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" .
}