@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY> .
@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:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_head {
   this: np:hasAssertion dgn-np:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_assertion ;
    np:hasProvenance dgn-np:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_provenance ;
    np:hasPublicationInfo dgn-np:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_assertion a np:Assertion .
  dgn-np:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_provenance a np:Provenance .
  dgn-np:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_assertion {
   miriam-gene:5979 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
  dgn-gda:DGNf5bd4c4dd0208ac8ef39962873bdd0cd sio:SIO_000628 miriam-gene:5979 , lld:C1527249 ;
    a sio:SIO_001121 .
}
dgn-np:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_provenance {
   dgn-np:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_assertion dcterms:description "[Using a proteomic-multiplexed analysis of the phosphotyrosine signaling together with antibody-based validation techniques, we identified several candidate molecules for RET (rearranged during transfection) tyrosine kinase receptor carrying mutations responsible for the multiple endocrine neoplasia type 2A and 2B (MEN2A and MEN2B) syndromes in two human medullary thyroid carcinoma (MTC) cell lines, TT and MZ-CRC-1, which express the RET-MEN2A and RET-MEN2B oncoproteins, respectively.]. 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:18756447 ;
    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:NP790264.RAXKnmcS4HV73mAziI4NfaLV9umpzdIwaWK1dgogj9XUY130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:05+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" .
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}