@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE> .
@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:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_head {
  this: np:hasAssertion dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_assertion ;
    np:hasProvenance dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_provenance ;
    np:hasPublicationInfo dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_assertion a np:Assertion .
  dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_provenance a np:Provenance .
  dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_assertion {
  miriam-gene:51741 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGNf977fa351524728410240ecad75545d0 sio:SIO_000628 miriam-gene:51741 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_provenance {
  dgn-np:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_assertion dcterms:description "[These findings together with other observations from literature on human cancers and the fact that the proline at codon 282 is extremely conserved in phylogenetically distant organisms (including Drosophila) suggest that the variant allele-282 could affect the biological function of WWOX, thereby predisposing individuals to thyroid cancer.]. 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:21520031 ;
    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:NP212409.RAZMmciG-yXudAzvjJwc8NCc8A5XLFBYUkpwkqp5C6LEE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+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" .
}