@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM
> .
@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/v3.0.0/void/
> .
dgn-np:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_head
{
this:
np:hasAssertion
dgn-np:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_assertion
;
np:hasProvenance
dgn-np:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_provenance
;
np:hasPublicationInfo
dgn-np:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_assertion
a
np:Assertion
.
dgn-np:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_provenance
a
np:Provenance
.
dgn-np:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_assertion
{
miriam-gene:1557
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN50e4b0a11e02d3c9ed0087a68e899ca2
sio:SIO_000628
miriam-gene:1557
,
lld:C0014544
;
a
sio:SIO_001122
.
}
dgn-np:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_provenance
{
dgn-np:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_assertion
dcterms:description
"[Among all the polymorphisms studied, functional variants from genes encoding CYP2C19, EPHX1, ABCB1 and SCN1A were highly polymorphic in North Indian epilepsy patients, and might account for differential drug response to first-line antiepileptic drugs.]. 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:20602612
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP81973.RABVbob4OOBxCGA7WQrgK_aj95qYM2MYjdcJtDY2Jm3HM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:25+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}