@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU> .
@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:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_head {
   this: np:hasAssertion dgn-np:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_assertion ;
    np:hasProvenance dgn-np:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_provenance ;
    np:hasPublicationInfo dgn-np:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_assertion a np:Assertion .
  dgn-np:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_provenance a np:Provenance .
  dgn-np:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_assertion {
   miriam-gene:54933 a ncit:C16612 .
  lld:C0276496 a ncit:C7057 .
  dgn-gda:DGN4335903ec1cb18809e64b49711f707fa sio:SIO_000628 miriam-gene:54933 , lld:C0276496 ;
    a sio:SIO_001121 .
}
dgn-np:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_provenance {
   dgn-np:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_assertion dcterms:description "[Formation of a high molecular weight complex of PS-1 composed of both endogenous PS-1 fragments may also explain the recent finding that FAD-associated mutations within the N-terminal portion of PS-1 result in the hyperaccumulation not only of the NTF but also of the CTF (Lee, M. K., Borchelt, D. R., Kim, G., Thinakaran, G., Slunt, H. H., Ratovitski, T., Martin, L. J., Kittur, A., Gandy, S., Levey, A. I., Jenkins, N., Copeland, N., Price, D. L., and Sisodia, S. S. (1997) Nat.]. 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:9452432 ;
    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:NP646944.RA29EahadUIHVrFiRkCcPWwqDKihzxV5PEitjTKuS-WUU130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:29+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> ;
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    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}