@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A> .
@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:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_head {
  this: np:hasAssertion dgn-np:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_assertion;
    np:hasProvenance dgn-np:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_provenance;
    np:hasPublicationInfo dgn-np:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_assertion a np:Assertion .
  
  dgn-np:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_provenance a np:Provenance .
  
  dgn-np:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_assertion {
  miriam-gene:23551 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN8bdabc7ebd5cd39eb63d2db722227051 sio:SIO_000628 miriam-gene:23551, lld:C0036341;
    a sio:SIO_001122 .
}

dgn-np:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_provenance {
  dgn-np:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_assertion dcterms:description
      "[Three of five candidate vulnerability genes (RASD2, APOL5, MYH9, EIF3S7, and CACNG2), which had marginally significant associations with schizophrenia, had significant associations with schizophrenic patients who did not have deficits in sustained attention on the undegraded CPT (RASD2 gene SNP rs736212; p = .0008 with single locus analysis) and the degraded CPT (MYH9 gene haplotype 1-1-1-1 of SNP rs3752463 - rs1557540 - rs713839 - rs739097; p = .0059 with haplotype analysis).]. 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:18571626;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP78102.RAMqQHTAAPIv7ykCVZGP11nEQqe2G2fluI81KaplXC01A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:38+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" .
}