@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis> .
@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:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_head {
  this: np:hasAssertion dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_assertion;
    np:hasProvenance dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_provenance;
    np:hasPublicationInfo dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_assertion a np:Assertion .
  
  dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_provenance a np:Provenance .
  
  dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_assertion {
  miriam-gene:2932 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN74e84ab2addadb315d7faf3e46c34117 sio:SIO_000628 miriam-gene:2932, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_provenance {
  dgn-np:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_assertion dcterms:description
      "[By using the Molecular Genetics of Schizophrenia data set, we were able to test and confirm that markers in NRXN1 and GSK3B have epistatic interactions in human populations that can jointly modulate risk of 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:22832527;
    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:NP559783.RAnYrSrZMrwKAobkcBJOoW-G6yfg6EIoqyX7gB4xmqKis130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:37+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}