@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8
> .
@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:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_head
{
this:
np:hasAssertion
dgn-np:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_assertion
;
np:hasProvenance
dgn-np:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_provenance
;
np:hasPublicationInfo
dgn-np:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_assertion
a
np:Assertion
.
dgn-np:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_provenance
a
np:Provenance
.
dgn-np:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_assertion
{
miriam-gene:1808
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGNf14506e6828c2e39af37f6143fb884cf
sio:SIO_000628
miriam-gene:1808
,
lld:C0085400
;
a
sio:SIO_001121
.
}
dgn-np:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_provenance
{
dgn-np:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_assertion
dcterms:description
"[Increased phosphorylation of CRMP2 is also apparent in mouse models of AD that express mutated AβPP and PSEN1, but not AβPP or tau alone, where it is detectable before the appearance of amyloid plaques and neurofibrillary tangles, suggesting it is an early event in AD pathogenesis.]. 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:21860090
;
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:NP868932.RAqCkXRmdg-innkzKT1uGHhqYYEOBn7fe28gPgtk4Rqi8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:51+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" .
}