@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM> .
@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:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_head {
  this: np:hasAssertion dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion;
    np:hasProvenance dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance;
    np:hasPublicationInfo dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion a np:Assertion .
  
  dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance a np:Provenance .
  
  dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion {
  miriam-gene:5027 a ncit:C16612 .
  
  lld:C0007115 a ncit:C7057 .
  
  dgn-gda:DGN9d65efde362a5f1f0dc8b4f333a03333 sio:SIO_000628 miriam-gene:5027, lld:C0007115;
    a sio:SIO_001122 .
}

dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_provenance {
  dgn-np:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_assertion dcterms:description
      "[A polymorphism in exon 13 of the P2X7 receptor gene at the +1513 position (Glu496Ala substitution, corresponding to SNP rs3751143) has been shown to eradicate the function of this receptor and has been correlated with histological variants and clinical parameters in thyroid cancer.]. 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:25178922;
    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:NP1215998.RAtho1MJHnLbi0-UML4UZNhWX_jPl6X2X-y9ODVSEpMcM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:57+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" .
}