@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik
> .
@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:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_head
{
this:
np:hasAssertion
dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_assertion
;
np:hasProvenance
dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_provenance
;
np:hasPublicationInfo
dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_assertion
a
np:Assertion
.
dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_provenance
a
np:Provenance
.
dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_assertion
{
miriam-gene:124935
a
ncit:C16612
.
lld:C2675211
a
ncit:C7057
.
dgn-gda:DGNaee7e30ba296350fb01fc65e1429a4f4
sio:SIO_000628
miriam-gene:124935
,
lld:C2675211
;
a
sio:SIO_001121
.
}
dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_provenance
{
dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_assertion
dcterms:description
"[Episodic ataxia type 6 represents the first human disease found to be associated with altered function of excitatory amino acid transporter anion channels and illustrates possible physiological and pathophysiological impacts of this functional mode of this class of glutamate transporters.]. 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:23107647
;
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:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:36+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" .
}