@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A
> .
@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:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_head
{
this:
np:hasAssertion
dgn-np:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_assertion
;
np:hasProvenance
dgn-np:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance
;
np:hasPublicationInfo
dgn-np:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_assertion
a
np:Assertion
.
dgn-np:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance
a
np:Provenance
.
dgn-np:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0085220
a
ncit:C7057
.
dgn-gda:DGN3836c23a8fe346347776e77d6231276f
sio:SIO_000628
miriam-gene:351
,
lld:C0085220
;
a
sio:SIO_001121
.
}
dgn-np:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_provenance
{
dgn-np:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_assertion
dcterms:description
"[Neuropathological changes associated with Alzheimer's disease (AD) such as amyloidplaques, cerebral amyloid angiopathy, and related pathologies are reproduced in APP23 transgenic mice overexpressing amyloid precursor protein (APP) with the Swedish mutation.]. 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:13679413
;
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:NP238806.RAblFCKW-Rflbene24DEZw0dBBSvVQVjuuKCqxGzZ_D0A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}