@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ> .
@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:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_head {
  this: np:hasAssertion dgn-np:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_assertion;
    np:hasProvenance dgn-np:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_provenance;
    np:hasPublicationInfo dgn-np:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_assertion a np:Assertion .
  
  dgn-np:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_provenance a np:Provenance .
  
  dgn-np:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_assertion {
  miriam-gene:1734 a ncit:C16612 .
  
  lld:C0014130 a ncit:C7057 .
  
  dgn-gda:DGN051355724cded79bae2ff5f6e9e45346 sio:SIO_000628 miriam-gene:1734, lld:C0014130;
    a sio:SIO_001122 .
}

dgn-np:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_provenance {
  dgn-np:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_assertion dcterms:description
      "[This new polymorphism in the 5'-UTR of D2 is associated with iodothyronine levels in blood donors, but not in elderly men. We hypothesize that this might be explained by the decline in skeletal muscle size during aging, resulting in a relative decrease in the contribution of D2 to serum T3 production.]. 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:15727947;
    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:NP45556.RAWv-7qb0cu_IY7okvFERkqaCx6k6j81ADrVwuyEP_KwQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}