@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg
> .
@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:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_head
{
this:
np:hasAssertion
dgn-np:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_assertion
;
np:hasProvenance
dgn-np:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_provenance
;
np:hasPublicationInfo
dgn-np:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_assertion
a
np:Assertion
.
dgn-np:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_provenance
a
np:Provenance
.
dgn-np:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_assertion
{
miriam-gene:627
a
ncit:C16612
.
lld:C0424605
a
ncit:C7057
.
dgn-gda:DGN81021a14ad5cb13ea4412d7b6dcf8d6c
sio:SIO_000628
miriam-gene:627
,
lld:C0424605
;
a
sio:SIO_001121
.
}
dgn-np:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_provenance
{
dgn-np:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_assertion
dcterms:description
"[CAPS2-deficient (CAPS2(-/-)) mice show reduced secretion of BDNF and NT-3; consequently, the cerebella of these mice exhibit developmental deficits, such as delayed development and increased cell death in GCs, fewer branched dendrites on Purkinje cells (PCs), and loss of the intercrural fissure.]. 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:19238500
;
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:NP282857.RAExJEPgTHzVNjCoQ18ghXzMbr6-zCrIZvHMMZet7ctqg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}