@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck
> .
@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:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_head
{
this:
np:hasAssertion
dgn-np:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_assertion
;
np:hasProvenance
dgn-np:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_provenance
;
np:hasPublicationInfo
dgn-np:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_assertion
a
np:Assertion
.
dgn-np:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_provenance
a
np:Provenance
.
dgn-np:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_assertion
{
miriam-gene:5663
a
ncit:C16612
.
lld:C0012644
a
ncit:C7057
.
dgn-gda:DGN05fc13e4497ad93342889e9b9d5d283a
sio:SIO_000628
miriam-gene:5663
,
lld:C0012644
;
a
sio:SIO_001121
.
}
dgn-np:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_provenance
{
dgn-np:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_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:NP27402.RAySy9mEoVg4FJUSQ1q2qxgLUghrfYUFG8N_34It2U5ck130_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" .
}