@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs> .
@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:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_head {
   this: np:hasAssertion dgn-np:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_assertion ;
    np:hasProvenance dgn-np:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance ;
    np:hasPublicationInfo dgn-np:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_assertion a np:Assertion .
  dgn-np:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance a np:Provenance .
  dgn-np:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_assertion {
   miriam-gene:1421 a ncit:C16612 .
  lld:C0238462 a ncit:C7057 .
  dgn-gda:DGN4320f731b634c0dbde14c2ba28ae3cb4 sio:SIO_000628 miriam-gene:1421 , lld:C0238462 ;
    a sio:SIO_001121 .
}
dgn-np:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_provenance {
   dgn-np:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_assertion dcterms:description "[We sequenced all the mutations as well as coding sequence regions of the 12 genes in an independent sample set including 35 medullary thyroid cancers (20 MEN2A) and 34 PCCs (22 MEN2A), but found no recurrent mutations.]. 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:25404689 ;
    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:NP1238110.RAlHvF5gAzT2EshKKhKovNGnir1PDh8DIl7nEeQiiuaDs130_publicationInfo {
   this: dcterms:created "2016-05-13T12:51:07+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" .
}