@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4> .
@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:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_head {
  this: np:hasAssertion dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_assertion;
    np:hasProvenance dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_provenance;
    np:hasPublicationInfo dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_assertion a np:Assertion .
  
  dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_provenance a np:Provenance .
  
  dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_assertion {
  miriam-gene:3159 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGN831f42007d326380f43edfe386c51bb8 sio:SIO_000628 miriam-gene:3159, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_provenance {
  dgn-np:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_assertion dcterms:description
      "[reported that the expression of the high mobility group (HMG) I(Y) proteins correlates with the malignant phenotype of human thyroid neoplasia, and suggested that the detection of the HMG I(Y) proteins might be a valid tool for an easy and sensitive discrimination assay between benign and malignant neoplastic thyroid disease.]. 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:10714095;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP810798.RAOVcCTyMhNj0VO6Py80cInmouh-KgzUOsZVpPuPnzql4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:17+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" .
}