@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY> .
@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:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_head {
  this: np:hasAssertion dgn-np:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_assertion ;
    np:hasProvenance dgn-np:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_provenance ;
    np:hasPublicationInfo dgn-np:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_assertion a np:Assertion .
  dgn-np:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_provenance a np:Provenance .
  dgn-np:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_assertion {
  miriam-gene:796 a ncit:C16612 .
  lld:C0025268 a ncit:C7057 .
  dgn-gda:DGNd2099779bdb100dd21c289a1538a4b9c sio:SIO_000628 miriam-gene:796 , lld:C0025268 ;
    a sio:SIO_001121 .
}
dgn-np:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_provenance {
  dgn-np:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_assertion dcterms:description "[Two individuals from two different MEN 2A kindreds were identified who had abnormal calcitonin stimulation tests but were not MEN 2A gene carriers by both linkage analysis and RET mutation analysis.]. 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:7909818 ;
    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:NP1326128.RAH4-a3eSGHYb_gzCSrZx3h-EQXeG4_92LDhR0gLjQEGY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:47+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" .
}