@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps> .
@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:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_head {
  this: np:hasAssertion dgn-np:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_assertion;
    np:hasProvenance dgn-np:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_provenance;
    np:hasPublicationInfo dgn-np:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_assertion a np:Assertion .
  
  dgn-np:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_provenance a np:Provenance .
  
  dgn-np:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_assertion {
  miriam-gene:213 a ncit:C16612 .
  
  lld:C0342185 a ncit:C7057 .
  
  dgn-gda:DGNf58b392c6c982f8df9993f71094f5cba sio:SIO_000628 miriam-gene:213, lld:C0342185;
    a sio:SIO_001121 .
}

dgn-np:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_provenance {
  dgn-np:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_assertion dcterms:description
      "[The characteristics of the albumin found in the affected members of this kindred are those we have defined for familial dysalbuminemic hyperthyroxinemia type I, which is inherited as an autosomal dominant trait.]. 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:3098776;
    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:NP1299979.RAkXas3CLdAH6jdBn8xiHhy3DQpjA__M5mcxAWnRAX_Ps130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:35+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" .
}