@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8> .
@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:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_head {
  this: np:hasAssertion dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_assertion ;
    np:hasProvenance dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_provenance ;
    np:hasPublicationInfo dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_assertion a np:Assertion .
  dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_provenance a np:Provenance .
  dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  lld:C0006118 a ncit:C7057 .
  dgn-gda:DGNe1455821fc3a48c9626250f30ca35ba1 sio:SIO_000628 miriam-gene:5624 , lld:C0006118 ;
    a sio:SIO_001121 .
}
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_provenance {
  dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_assertion dcterms:description "[The authors analyzed their established hereditary CRC Registry for brain tumors in FAP pedigrees (56 families, 213 individuals), pooled their patients with BTP and known APC mutations with those reported thus far elsewhere, and compared the resulting mutation distribution of FAP-BTP with the mutation distribution for APC mutations in the US.]. 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:17238184 ;
    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:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:17+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> ;
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}