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http://rdf.disgenet.org/nanopublications.trig#NP359540.RA3co2Daw2QS4iDYeAb22I_HL1NleIcekGGQpVtzkcstI
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP359540.RA3co2Daw2QS4iDYeAb22I_HL1NleIcekGGQpVtzkcstI130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP359540.RA3co2Daw2QS4iDYeAb22I_HL1NleIcekGGQpVtzkcstI130_assertion
a
np:Assertion
.
dgn-np:NP359540.RA3co2Daw2QS4iDYeAb22I_HL1NleIcekGGQpVtzkcstI130_provenance
a
np:Provenance
.
dgn-np:NP359540.RA3co2Daw2QS4iDYeAb22I_HL1NleIcekGGQpVtzkcstI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP359540.RA3co2Daw2QS4iDYeAb22I_HL1NleIcekGGQpVtzkcstI130_assertion
{
miriam-gene:9211
a
ncit:C16612
.
lld:C0393682
a
ncit:C7057
.
dgn-gda:DGN02c39945b9ee3b2e28a2e9e051e39fd2
sio:SIO_000628
miriam-gene:9211
,
lld:C0393682
;
a
sio:SIO_001121
.
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dgn-np:NP359540.RA3co2Daw2QS4iDYeAb22I_HL1NleIcekGGQpVtzkcstI130_provenance
{
dgn-np:NP359540.RA3co2Daw2QS4iDYeAb22I_HL1NleIcekGGQpVtzkcstI130_assertion
dcterms:description
"[Furthermore, previous knowledge on molecular disease mechanisms of related LGI proteins, for example LGI1 and autosomal dominant lateral temporal epilepsy, could be applied to deepen the understanding of the PEPS disease mechanism at the molecular level, which may facilitate therapeutic intervention in the future.]. 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:20183877
;
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 .
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dgn-np:NP359540.RA3co2Daw2QS4iDYeAb22I_HL1NleIcekGGQpVtzkcstI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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
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pav:authoredBy
<
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> , <
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> , <
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> , <
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
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"v2.1.0" .
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