@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE> .
@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:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_head {
  this: np:hasAssertion dgn-np:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_assertion;
    np:hasProvenance dgn-np:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_provenance;
    np:hasPublicationInfo dgn-np:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_assertion a np:Assertion .
  
  dgn-np:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_provenance a np:Provenance .
  
  dgn-np:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_assertion {
  miriam-gene:5979 a ncit:C16612 .
  
  lld:C0019569 a ncit:C7057 .
  
  dgn-gda:DGN08607214b8583412b6392bc4e6eb91d6 sio:SIO_000628 miriam-gene:5979, lld:C0019569;
    a sio:SIO_001121 .
}

dgn-np:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_provenance {
  dgn-np:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_assertion dcterms:description
      "[Results showed the benefit of systematic RET mutation screening in HD patients in order to identify the risk of MTC in preclinical stage of the disease in patients with HD and their family members.]. 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:17021738;
    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:NP229546.RAAWA7i_WG2wBOwgCwUaWUE9pLZ-d5LIm7SVQhQpxD3RE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:09+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" .
}