@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM
> .
@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:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_head
{
this:
np:hasAssertion
dgn-np:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_assertion
;
np:hasProvenance
dgn-np:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_provenance
;
np:hasPublicationInfo
dgn-np:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_assertion
a
np:Assertion
.
dgn-np:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_provenance
a
np:Provenance
.
dgn-np:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_assertion
{
miriam-gene:3778
a
ncit:C16612
.
lld:C0008489
a
ncit:C7057
.
dgn-gda:DGN87694f94a4e3bee398f933692a70bfc8
sio:SIO_000628
miriam-gene:3778
,
lld:C0008489
;
a
sio:SIO_001122
.
}
dgn-np:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_provenance
{
dgn-np:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_assertion
dcterms:description
"[mutated in generalized epilepsy and paroxysmal dyskinesia and have implications for the pathogenesis of human epilepsy, the neurophysiology of paroxysmal movement disorders and the role of BK channels in neurological disease ]. 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:15937479
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP150688.RAV4CmfEoydpqnRDty1wBMl8Tio4T8roKeeKUUoj6cGRM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:20+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" .
}