@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA> .
@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:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_head {
  this: np:hasAssertion dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_assertion;
    np:hasProvenance dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_provenance;
    np:hasPublicationInfo dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_assertion a np:Assertion .
  
  dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_provenance a np:Provenance .
  
  dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_assertion {
  miriam-gene:10849 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN8da43e5802a508dd44c0e9045f656764 sio:SIO_000628 miriam-gene:10849, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_provenance {
  dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_assertion dcterms:description
      "[Using Computed Associations in Sequential Text (CAST) software to quantify the frequency of such associations in speech, we have reported more frequent normative associations in language samples from patients with schizophrenia and in individuals with schizotypal characteristics.]. 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:22819779;
    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:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:02+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" .
}