@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo
> .
@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:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_head
{
this:
np:hasAssertion
dgn-np:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_assertion
;
np:hasProvenance
dgn-np:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_provenance
;
np:hasPublicationInfo
dgn-np:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_assertion
a
np:Assertion
.
dgn-np:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_provenance
a
np:Provenance
.
dgn-np:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_assertion
{
miriam-gene:773
a
ncit:C16612
.
lld:C0234131
a
ncit:C7057
.
dgn-gda:DGNf42b3ab9907d63dadd879d7bd4b895ba
sio:SIO_000628
miriam-gene:773
,
lld:C0234131
;
a
sio:SIO_001121
.
}
dgn-np:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_provenance
{
dgn-np:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_assertion
dcterms:description
"[Moreover, the review describes different ataxic spontaneous cacna1a mouse mutants and the important insights into the cerebellar mechanisms underlying motor dysfunction caused by mutant CaV2.1 channels that were obtained from their functional characterization.]. 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:20204399
;
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:NP787144.RALcNmbBucqZL2MXjVbjG4D10rpGoWFp-Q_Qm5GJeiCEo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}