@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs> .
@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/v3.0.0/void/> .

dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_head {
  this: np:hasAssertion dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_assertion;
    np:hasProvenance dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_provenance;
    np:hasPublicationInfo dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_assertion a np:Assertion .
  
  dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_provenance a np:Provenance .
  
  dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_assertion {
  miriam-gene:139818 a ncit:C16612 .
  
  lld:C0025269 a ncit:C7057 .
  
  dgn-gda:DGN84f723f6e92ce6b6a26390391d3d6915 sio:SIO_000628 miriam-gene:139818, lld:C0025269;
    a sio:SIO_001121 .
}

dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_provenance {
  dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_assertion dcterms:description
      "[The most important mutation associated with Multiple Endocrine Neoplasia type 2B (MEN 2B) is the change of thymine to cytosine in codon 918 of exon 16 in the RET oncogene (ATG → ACG).]. 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:21253810;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:34+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}