@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs> .
@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:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_head {
   this: np:hasAssertion dgn-np:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_assertion ;
    np:hasProvenance dgn-np:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_provenance ;
    np:hasPublicationInfo dgn-np:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_assertion a np:Assertion .
  dgn-np:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_provenance a np:Provenance .
  dgn-np:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_assertion {
   miriam-gene:5979 a ncit:C16612 .
  lld:C0019569 a ncit:C7057 .
  dgn-gda:DGN313b5c8cc62f41874d135acc4bf03ff5 sio:SIO_000628 miriam-gene:5979 , lld:C0019569 ;
    a sio:SIO_001121 .
}
dgn-np:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_provenance {
   dgn-np:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_assertion dcterms:description "[RET is a receptor tyrosine kinase gene which is responsible for three different inherited cancer syndromes namely multiple endocrine neoplasia type 2A (MEN 2A), type 2B (MEN 2B) and familial medullary thyroid carcinoma (FMTC) as well as for Hirschsprung disease (HSCR), a congenital disorder affecting the intestinal motility.]. 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:7784092 ;
    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:NP1321727.RAJxU4Z4uUawuWo_oi4hbHv22y8VGDND39ekq7qrswNDs130_publicationInfo {
   this: dcterms:created "2016-05-13T12:51:45+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" .
}