@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ> .
@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:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_head {
  this: np:hasAssertion dgn-np:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_assertion ;
    np:hasProvenance dgn-np:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_assertion a np:Assertion .
  dgn-np:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_provenance a np:Provenance .
  dgn-np:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_assertion {
  miriam-gene:5300 a ncit:C16612 .
  lld:C0236642 a ncit:C7057 .
  dgn-gda:DGN40ab995b2d04565a2ef6d0f8211b206a sio:SIO_000628 miriam-gene:5300 , lld:C0236642 ;
    a sio:SIO_001121 .
}
dgn-np:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_provenance {
  dgn-np:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_assertion dcterms:description "[Analysis of eighteen PIN1 common polymorphisms and their haplotypes in EOAD, LOAD and FTD individuals in comparison with the control group did not reveal their contribution to disease risk.In six unrelated familial AD patients four novel PIN1 sequence variants were detected.]. 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:19909517 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP625974.RA1QChCUCzlH5jvms4B4N0jGowhDItVf4ZThcT4vXm0HQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:54+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" .
}