@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU> .
@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:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_head {
  this: np:hasAssertion dgn-np:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_assertion;
    np:hasProvenance dgn-np:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_provenance;
    np:hasPublicationInfo dgn-np:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_assertion a np:Assertion .
  
  dgn-np:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_provenance a np:Provenance .
  
  dgn-np:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_assertion {
  miriam-gene:54329 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_provenance {
  dgn-np:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_assertion dcterms:description
      "[These data suggest that risk-associated variants in SREB2 are associated with phenotypes similar to those found in patients with schizophrenia in the DLPFC and the amygdala of males, while the pattern is opposite in females.]. 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:22968816;
    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:NP275899.RAnxFMIwcLI2nikq0qn-zoehMI9Mc7LkDdRlbRFZeT4HU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:35+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" .
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