@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw
> .
@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:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_head
{
this:
np:hasAssertion
dgn-np:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_assertion
;
np:hasProvenance
dgn-np:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_provenance
;
np:hasPublicationInfo
dgn-np:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_assertion
a
np:Assertion
.
dgn-np:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_provenance
a
np:Provenance
.
dgn-np:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_assertion
{
miriam-gene:23385
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN75b7ca08821538be7f2ceaeb656f1ac1
sio:SIO_000628
miriam-gene:23385
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_provenance
{
dgn-np:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_assertion
dcterms:description
"[Furthermore, we found an intronic +17G>C polymorphism in PEN2 which, in homozygous form, was greater in early onset Alzheimer's disease (EOAD) compared to controls, and one haplotype in the NCSTN gene which was linked to EOAD and familial AD (FAD).]. 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:16423463
;
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:NP473032.RA6zqmbElV5m4ze84csZ6FDItaHFZJtx-y38ddhyO-fBw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+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" .
}