@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg> .
@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:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_head {
  this: np:hasAssertion dgn-np:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_assertion ;
    np:hasProvenance dgn-np:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_provenance ;
    np:hasPublicationInfo dgn-np:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_assertion a np:Assertion .
  dgn-np:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_provenance a np:Provenance .
  dgn-np:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_assertion {
  miriam-gene:114568 a ncit:C16612 .
  lld:C0238462 a ncit:C7057 .
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dgn-np:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_provenance {
  dgn-np:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_assertion dcterms:description "[We used linkage analysis to test the significance of two of the known susceptibility loci for fNMTC, TCO on 19p13 and NMTC1 on 2q21 in 10 fNMTC families, nine of which present with cell oxyphilia, a rare histological phenotype associated with TCO.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP172183.RAkuyO9UelXVdUKExtaMELTL2OWlfQVwvc6sGeEoU46Cg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:33+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 ;
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}