@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts> .
@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:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_head {
  this: np:hasAssertion dgn-np:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_assertion ;
    np:hasProvenance dgn-np:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_provenance ;
    np:hasPublicationInfo dgn-np:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_assertion a np:Assertion .
  dgn-np:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_provenance a np:Provenance .
  dgn-np:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_assertion {
  miriam-gene:8878 a ncit:C16612 .
  lld:C0029401 a ncit:C7057 .
  dgn-gda:DGNe148be26342224c1fb4edbfc9624cba5 sio:SIO_000628 miriam-gene:8878 , lld:C0029401 ;
    a sio:SIO_001122 .
}
dgn-np:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_provenance {
  dgn-np:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_assertion dcterms:description "[Even though our findings suggest a minor involvement of the SQSTM1 gene in the pathogenesis of sporadic Italian Paget's cases, the identification of different significant mutations within the SQSTM1 gene in unrelated, but clinically similar individuals, offers extremely convincing evidence for a causal relationship between this gene and PDB.]. 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:15125799 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP62136.RACWp3IvHr4fSv2g_EXzczcdlH3J7DuPNZJhE-UrM8Lts130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}