@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM> .
@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/v3.0.0/void/> .
dgn-np:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_head {
  this: np:hasAssertion dgn-np:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_assertion ;
    np:hasProvenance dgn-np:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_provenance ;
    np:hasPublicationInfo dgn-np:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_assertion a np:Assertion .
  dgn-np:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_provenance a np:Provenance .
  dgn-np:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_assertion {
  miriam-gene:324 a ncit:C16612 .
  lld:C0017097 a ncit:C7057 .
  dgn-gda:DGN4380c1f074e9ab790eb2f43210da53ae sio:SIO_000628 miriam-gene:324 , lld:C0017097 ;
    a sio:SIO_001122 .
}
dgn-np:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_provenance {
  dgn-np:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_assertion dcterms:description "[This disorder was regarded as a separate disease until the identification of the APC gene when it was recognized that mutations in the APC gene were the underlying cause of both Gardner syndrome and familial adenomatous polyposis (FAP).]. 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:16411234 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP136821.RASHKsbgQQU888xlciy4rTMWpNAmbVq77R-KjOFGQ3rhM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:56+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}