@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU
> .
@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:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_head
{
this:
np:hasAssertion
dgn-np:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_assertion
;
np:hasProvenance
dgn-np:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_provenance
;
np:hasPublicationInfo
dgn-np:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_assertion
a
np:Assertion
.
dgn-np:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_provenance
a
np:Provenance
.
dgn-np:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_assertion
{
miriam-gene:1509
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGNceeef14ae3cbc326869a1eccca17e51f
sio:SIO_000628
miriam-gene:1509
,
lld:C0085400
;
a
sio:SIO_001121
.
}
dgn-np:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_provenance
{
dgn-np:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_assertion
dcterms:description
"[This reduction of expression of messages related to growth of neuronal processes and to synapses is selective, because expression of message for the lysosomal enzyme, cathepsin D, is increased in neurons containing NFTs.]. 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:9562477
;
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:NP725091.RAAqLLYvYZb_3tnf41AG9pcce89y88wJsf9ZKa_GObJBU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}