@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E> .
@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 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:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_head {
  this: np:hasAssertion dgn-np:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_assertion;
    np:hasProvenance dgn-np:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_provenance;
    np:hasPublicationInfo dgn-np:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_assertion a np:Assertion .
  
  dgn-np:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_provenance a np:Provenance .
  
  dgn-np:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_assertion {
  miriam-gene:3274 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN2335da9579e79ec77efd313d5fb3de5a sio:SIO_000628 miriam-gene:3274, lld:C0036341;
    a sio:SIO_001122 .
}

dgn-np:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_provenance {
  dgn-np:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_assertion dct:description
      "[We have concluded that the participation of these variants in the disorder is unlikely, particularly in view of their apparent lack of function and unlikely influence on receptor expression. However their nature alludes to the potential presence of other more important alterations further along these regions, where sequences encoding alternate promoters have recently been identified for each receptor that may yet be found to harbour such polymorphisms.]. 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:12429384;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP57543.RAzuhz3IAzYQj52vE6f-RRd9V1QrUFKPZqcGI5RzSqH5E130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}