@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc
> .
@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/v4.0.0/void/
> .
dgn-np:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_head
{
this:
np:hasAssertion
dgn-np:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_assertion
;
np:hasProvenance
dgn-np:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_provenance
;
np:hasPublicationInfo
dgn-np:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_assertion
a
np:Assertion
.
dgn-np:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_provenance
a
np:Provenance
.
dgn-np:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_assertion
{
miriam-gene:3708
a
ncit:C16612
.
lld:C0004134
a
ncit:C7057
.
dgn-gda:DGN919e72309563d5bd5374586cfb202a51
sio:SIO_000628
miriam-gene:3708
,
lld:C0004134
;
a
sio:SIO_001121
.
}
dgn-np:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_provenance
{
dgn-np:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_assertion
dcterms:description
"[Because of this distinct role of each isoform of IP3R, the dysregulation of IP3 receptor causes various kinds of diseases in human and rodents such as ataxia, vulnerability to neuronal degeneration, heart disease, exocrine secretion deficit, taste perception deficit.]. 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:25497594
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1247021.RA4jsk-3_zQW7et4_dQj9Z51yaJNDpYCR4KF3OsgkCNNc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:11+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}