@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI> .
@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:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_head {
  this: np:hasAssertion dgn-np:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_assertion;
    np:hasProvenance dgn-np:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_provenance;
    np:hasPublicationInfo dgn-np:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_assertion a np:Assertion .
  
  dgn-np:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_provenance a np:Provenance .
  
  dgn-np:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_assertion {
  miriam-gene:5979 a ncit:C16612 .
  
  lld:C0025268 a ncit:C7057 .
  
  dgn-gda:DGNdbdab0ec8ed807fc965b4c2c00fe10c6 sio:SIO_000628 miriam-gene:5979, lld:C0025268;
    a sio:SIO_001121 .
}

dgn-np:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_provenance {
  dgn-np:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_assertion dcterms:description
      "[A deeper understanding of the molecular signaling of normal versus abnormal RET activity in cancer will enable the development of potential new treatments for patients with sporadic and inherited thyroid cancer or MEN 2 syndrome.]. 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:15982921;
    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:NP501242.RA70_b2rWYK2S-n4DwdoTpjhOSfv0pQ3Lv_oKHYDKpbUI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:32+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" .
}