@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U> .
@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:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_head {
  this: np:hasAssertion dgn-np:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_assertion;
    np:hasProvenance dgn-np:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_provenance;
    np:hasPublicationInfo dgn-np:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_assertion a np:Assertion .
  
  dgn-np:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_provenance a np:Provenance .
  
  dgn-np:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_assertion {
  miriam-gene:491 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGN22d8ab7446ce787f133c2eb271a3186f sio:SIO_000628 miriam-gene:491, lld:C0004352;
    a sio:SIO_001121 .
}

dgn-np:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_provenance {
  dgn-np:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_assertion dcterms:description
      "[These results provide converging evidence for an association between ATP2B2 gene variants and autism in male subjects, spurring interest into the identification of functional variants, most likely involved in the homeostasis of Ca2+ signaling.]. 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:21757185;
    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:NP285717.RAByYvSAClwtaqbAEij_hWYiRUWCpiqCD3XwhhpbbNl5U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:41+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" .
}