@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8> .
@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:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_head {
  this: np:hasAssertion dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_assertion;
    np:hasProvenance dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_provenance;
    np:hasPublicationInfo dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_assertion a np:Assertion .
  
  dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_provenance a np:Provenance .
  
  dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_assertion {
  miriam-gene:5979 a ncit:C16612 .
  
  lld:C1833921 a ncit:C7057 .
  
  dgn-gda:DGN2075c2ea97c51b99b29b0a8b8a684a81 sio:SIO_000628 miriam-gene:5979, lld:C1833921;
    a sio:SIO_001121 .
}

dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_provenance {
  dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_assertion dcterms:description
      "[In multiple endocrine neoplasia type 2A (MEN 2A) and familial medullary thyroid cancer (FMTC), the majority of germline mutations are restricted to specific positions in exons 10 and 11 of the RET gene.]. 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:12694233;
    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:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}