@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8> .
@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:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_head {
  this: np:hasAssertion dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_assertion ;
    np:hasProvenance dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_provenance ;
    np:hasPublicationInfo dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_assertion a np:Assertion .
  dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_provenance a np:Provenance .
  dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_assertion {
  miriam-gene:1869 a ncit:C16612 .
  lld:C0030521 a ncit:C7057 .
  dgn-gda:DGN438bd5407ad1e9323d5786cf84c4c713 sio:SIO_000628 miriam-gene:1869 , lld:C0030521 ;
    a sio:SIO_001121 .
}
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_provenance {
  dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_assertion dcterms:description "[Furthermore, the locus that codes for a distinct phenotype, medullary thyroid carcinoma (MTC) with parathyroid tumors (PTs) and no pheochromocytomas (PHEOs) (referred to as MTC with PTs), in one of the families was closely linked to two markers, D10Z1 and RBP3, with lodscores of 2.86 and 3.54, respectively, at theta = 0.]. 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:1978560 ;
    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:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:28+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" .
}