@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg> .
@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:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_head {
  this: np:hasAssertion dgn-np:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_assertion ;
    np:hasProvenance dgn-np:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_provenance ;
    np:hasPublicationInfo dgn-np:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_assertion a np:Assertion .
  dgn-np:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_provenance a np:Provenance .
  dgn-np:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_assertion {
  miriam-gene:7031 a ncit:C16612 .
  lld:C0497327 a ncit:C7057 .
  dgn-gda:DGN0a901cf95ff3db3f762b2d513e165ca9 sio:SIO_000628 miriam-gene:7031 , lld:C0497327 ;
    a sio:SIO_001121 .
}
dgn-np:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_provenance {
  dgn-np:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_assertion dcterms:description "[Eleven early-onset dementia families, all with affected individuals who have either presented clinical symptoms of early onset familial Alzheimer's disease (EOFAD) or have been confirmed to have EOFAD by autopsy, and two early onset cases with biopsy-confirmed AD pathology, were screened for missense mutations in the entire coding region of presenilin-1 (PS-1) and -2 (PS-2) genes.]. 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:9172170 ;
    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:NP354379.RA1zycolf5vxihKd_tw_GEaZEJ40qVjdMsLfPP-EbP8vg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:28+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" .
}