@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c> .
@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:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_head {
  this: np:hasAssertion dgn-np:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_assertion;
    np:hasProvenance dgn-np:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_provenance;
    np:hasPublicationInfo dgn-np:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_assertion a np:Assertion .
  
  dgn-np:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_provenance a np:Provenance .
  
  dgn-np:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_assertion {
  miriam-gene:4489 a ncit:C16612 .
  
  lld:C1707446 a ncit:C7057 .
  
  dgn-gda:DGN9fbfa260ed3e63d3d9c7ce9cc435a3af sio:SIO_000628 miriam-gene:4489, lld:C1707446;
    a sio:SIO_001121 .
}

dgn-np:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_provenance {
  dgn-np:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_assertion dcterms:description
      "[Although common RET mutations providing evidence of familial forms of MTC were identified in only 3 of 16 families, clinical and histologic features usually seen in inherited forms of MTC such as young age of occurrence, bilateral CCH or associated case in family were found in 11 of the remaining 14 patients.]. 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:15588381;
    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:NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:28+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" .
}