@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_head
{
this:
np:hasAssertion
dgn-np:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_assertion
;
np:hasProvenance
dgn-np:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_provenance
;
np:hasPublicationInfo
dgn-np:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_assertion
a
np:Assertion
.
dgn-np:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_provenance
a
np:Provenance
.
dgn-np:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_assertion
{
miriam-gene:767
a
ncit:C16612
.
lld:C0004134
a
ncit:C7057
.
dgn-gda:DGN6e2692530c459dc3b650158054622a1c
sio:SIO_000628
miriam-gene:767
,
lld:C0004134
;
a
sio:SIO_001121
.
}
dgn-np:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_provenance
{
dgn-np:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_assertion
dcterms:description
"[A mutation in the CA8 gene has been associated with ataxia, mild mental retardation and quadrupedal gait in humans and with lifelong gait disorder in mice, suggesting an important role for CARP VIII in the brain.]. 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:20819067
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP276575.RAlEd3EX2x_p_RAIvSgEo8ebvf_R5zU63DZF49i42s2GM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:17+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}