@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ
> .
@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:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_head
{
this:
np:hasAssertion
dgn-np:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_assertion
;
np:hasProvenance
dgn-np:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_assertion
a
np:Assertion
.
dgn-np:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_provenance
a
np:Provenance
.
dgn-np:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_assertion
{
miriam-gene:338399
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGN1e5f4bdff1132ae18358cd7d21b5db22
sio:SIO_000628
miriam-gene:338399
,
lld:C0497327
;
a
sio:SIO_001121
.
}
dgn-np:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_provenance
{
dgn-np:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_assertion
dcterms:description
"[Serial examinations, PET scans, and autopsy revealed that the mutation in this highly conserved portion of PS1 causes an aggressive dementia that maintains the usual regional hierarchy of disease pathology while extending abnormalities into more widespread brain areas than typically seen in AD.]. 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:15159497
;
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:NP431696.RAChqusUuishm27Ii3ejpE5GvSrrJFBsHXn37-3AmQMAQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}