@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM
> .
@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:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_head
{
this:
np:hasAssertion
dgn-np:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_assertion
;
np:hasProvenance
dgn-np:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_provenance
;
np:hasPublicationInfo
dgn-np:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_assertion
a
np:Assertion
.
dgn-np:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_provenance
a
np:Provenance
.
dgn-np:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_assertion
{
miriam-gene:1514
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGNfc3e743b620c93174f3a72e468e9ff4b
sio:SIO_000628
miriam-gene:1514
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_provenance
{
dgn-np:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_assertion
dcterms:description
"[Human CTSL is expressed in the brain of these compound mutants, predominantly in neurons of the cerebral cortex and in Purkinje cells of the cerebellum, where it appears to prevent neuronal cell death.]. 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:16913838
;
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:NP670706.RAACJW2Ww5Hb0VOcF1L26E1cbhM7hnXnVGnmvIyuko0cM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}