@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs
> .
@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:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_head
{
this:
np:hasAssertion
dgn-np:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_assertion
;
np:hasProvenance
dgn-np:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_provenance
;
np:hasPublicationInfo
dgn-np:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_assertion
a
np:Assertion
.
dgn-np:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_provenance
a
np:Provenance
.
dgn-np:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_assertion
{
miriam-gene:1808
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGN614995707541c24b86c6f52570162ee4
sio:SIO_000628
miriam-gene:1808
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_provenance
{
dgn-np:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_assertion
dcterms:description
"[Indeed, phosphorylation of CRMP2, at the residues targeted by GSK3 and Cdk5, is relatively high in cortex isolated from human AD brain, as well as in the brains of animal models of AD, while phospho-CRMP2 is found in neurofibrillary tangles.]. 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:19519308
;
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:NP519045.RAtn1q1O4-qPZfEKhr2OUe-31gbA8djYEHmXkSpEDtFgs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:09+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" .
}