@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU> .
@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:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_head {
  this: np:hasAssertion dgn-np:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_assertion;
    np:hasProvenance dgn-np:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_provenance;
    np:hasPublicationInfo dgn-np:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_assertion a np:Assertion .
  
  dgn-np:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_provenance a np:Provenance .
  
  dgn-np:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_assertion {
  miriam-gene:3710 a ncit:C16612 .
  
  lld:C0004134 a ncit:C7057 .
  
  dgn-gda:DGN8bc2c2687ab35593822dafb3f4352f9c sio:SIO_000628 miriam-gene:3710, lld:C0004134;
    a sio:SIO_001121 .
}

dgn-np:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_provenance {
  dgn-np:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_assertion dcterms:description
      "[Because of this distinct role of each isoform of IP3R, the dysregulation of IP3 receptor causes various kinds of diseases in human and rodents such as ataxia, vulnerability to neuronal degeneration, heart disease, exocrine secretion deficit, taste perception deficit.]. 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:25497594;
    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:NP1247022.RAU_Lo6SUKT5HIC5hsNHbfBgQSRAF54itsGSIKL-FXoAU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:11+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>,
      <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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}