@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo
> .
@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:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_head
{
this:
np:hasAssertion
dgn-np:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_assertion
;
np:hasProvenance
dgn-np:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_provenance
;
np:hasPublicationInfo
dgn-np:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_assertion
a
np:Assertion
.
dgn-np:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_provenance
a
np:Provenance
.
dgn-np:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_assertion
{
miriam-gene:322
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN63c30143bbaab5b463bf43823a982028
sio:SIO_000628
miriam-gene:322
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_provenance
{
dgn-np:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_assertion
dcterms:description
"[Genet., 103 (1998) 295) recently reported that a deletion polymorphism in intron 13 of the FE65 gene may be protective for sporadic Alzheimer's disease (AD) forms and suggested that this deletion may modify splicing between exon 13 and 14 (the two exons encoding the interaction domain of FE65 with APP).]. 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:11065130
;
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:NP624846.RAkuVx74kgzlzztsOzg3LX-HQ2uVFLx0LmkmFyarheBXo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:17+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" .
}