@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_head {
  this: np:hasAssertion dgn-np:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_assertion;
    np:hasProvenance dgn-np:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_provenance;
    np:hasPublicationInfo dgn-np:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_assertion a np:Assertion .
  
  dgn-np:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_provenance a np:Provenance .
  
  dgn-np:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_assertion {
  miriam-gene:55840 a ncit:C16612 .
  
  lld:C0004936 a ncit:C7057 .
  
  dgn-gda:DGN63beb857ad25834652ce3909ba95b004 sio:SIO_000628 miriam-gene:55840, lld:C0004936;
    a sio:SIO_001121 .
}

dgn-np:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_provenance {
  dgn-np:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_assertion dcterms:description
      "[Endophenotypes, traits genetically correlated with an illness, can help characterize the impact of risk genes by providing genetically relevant traits that are more tractable than the behavioral symptoms that classify mental illness.]. 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:25168609;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1214682.RADTanMOxVk2XjQeX_bjERRNiPgbNs7hYU-f6OX1x3HFI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:56+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}