@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ
> .
@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:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_head
{
this:
np:hasAssertion
dgn-np:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_assertion
;
np:hasProvenance
dgn-np:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_assertion
a
np:Assertion
.
dgn-np:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_provenance
a
np:Provenance
.
dgn-np:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_assertion
{
miriam-gene:5663
a
ncit:C16612
.
lld:C0276496
a
ncit:C7057
.
dgn-gda:DGN21a446eab3ea3b05d02e1abf10a53a19
sio:SIO_000628
miriam-gene:5663
,
lld:C0276496
;
a
sio:SIO_001121
.
}
dgn-np:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_provenance
{
dgn-np:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_assertion
dcterms:description
"[Here, we generated a double homozygous knock-in mouse model that incorporates the Swedish familial Alzheimer's disease mutations and converts mouse Abeta to the human sequence in amyloid precursor protein and had the P264L familial Alzheimer's disease mutation in presenilin-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:16651627
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP27395.RAcsPCHMo7gzixhzd7UOtF69TvVJhwSI-sf7V8pCnEggQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:11+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" .
}