@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4> .
@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:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_head {
  this: np:hasAssertion dgn-np:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_assertion;
    np:hasProvenance dgn-np:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_provenance;
    np:hasPublicationInfo dgn-np:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_assertion a np:Assertion .
  
  dgn-np:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_provenance a np:Provenance .
  
  dgn-np:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_assertion {
  miriam-gene:775 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN0180d8f8ddd59f659da58f3ebeaca532 sio:SIO_000628 miriam-gene:775, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_provenance {
  dgn-np:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_assertion dcterms:description
      "[Genetic variation in CACNA1C have also been associated with depression, schizophrenia, autism spectrum disorders, as well as changes in brain function and structure in control subjects who have no diagnosable psychiatric 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:22705413;
    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:NP221527.RAfXF9QhwgX5O1B0Pg9wKNbiWqyqqOoUpgH3gGkC33JV4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:03+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" .
}