@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg> .
@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:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_head {
  this: np:hasAssertion dgn-np:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_assertion;
    np:hasProvenance dgn-np:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_provenance;
    np:hasPublicationInfo dgn-np:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_assertion a np:Assertion .
  
  dgn-np:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_provenance a np:Provenance .
  
  dgn-np:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_assertion {
  miriam-gene:5979 a ncit:C16612 .
  
  lld:C0025268 a ncit:C7057 .
  
  dgn-gda:DGNe8e2f73df6bf7261f0224d32b6dceeee sio:SIO_000628 miriam-gene:5979, lld:C0025268;
    a sio:SIO_001122 .
}

dgn-np:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_provenance {
  dgn-np:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_assertion dcterms:description
      "[In 46 cases of sporadic MTCs, we also studied the cosegregation of somatic RET gene mutation and G691S polymorphism as well as the linkage of the polymorphism with RET germline mutation in 60 members of eight multiple endocrine neoplasia type 2 families.]. 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:15240649;
    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:NP451147.RAvtHqUkZ_e-RMuiKVnsZVwoga9BOIs-7cxSj6klw9QDg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:09+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: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" .
}