@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc
> .
@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:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_head
{
this:
np:hasAssertion
dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_assertion
;
np:hasProvenance
dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_provenance
;
np:hasPublicationInfo
dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_assertion
a
np:Assertion
.
dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_provenance
a
np:Provenance
.
dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_assertion
{
miriam-gene:1471
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGNabb8455c9cbb56b92ee7a565224c88d8
sio:SIO_000628
miriam-gene:1471
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_provenance
{
dgn-np:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_assertion
dcterms:description
"[Crossbreeding of CysBKO mice with either CysC-overexpressing transgenic mice or CysC-knockout mice demonstrates that clinical symptoms and neuropathologies, including motor coordination disorder, cerebellar atrophy, neuronal loss in the cerebellum and cerebral cortex, and gliosis caused by CysB deficiency, are rescued by CysC overexpression and exacerbated by CysC deficiency.]. 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:20889561
;
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:NP164389.RAmykPFhc00O-2R3TTFOV7psPqsP36XEUvG-4k69fP2nc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}