@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP262896.RAod_mIpvuX0CTa55mEHWLSeJXX6i4nSLPr1C1DNmiLkY
> .
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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#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP262896.RAod_mIpvuX0CTa55mEHWLSeJXX6i4nSLPr1C1DNmiLkY130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP262896.RAod_mIpvuX0CTa55mEHWLSeJXX6i4nSLPr1C1DNmiLkY130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP262896.RAod_mIpvuX0CTa55mEHWLSeJXX6i4nSLPr1C1DNmiLkY130_assertion
a
np:Assertion
.
dgn-np:NP262896.RAod_mIpvuX0CTa55mEHWLSeJXX6i4nSLPr1C1DNmiLkY130_provenance
a
np:Provenance
.
dgn-np:NP262896.RAod_mIpvuX0CTa55mEHWLSeJXX6i4nSLPr1C1DNmiLkY130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:7368
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN3ffe7e43073dfb3b6497e475b8abcfce
sio:SIO_000628
miriam-gene:7368
,
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;
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.
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dgn-np:NP262896.RAod_mIpvuX0CTa55mEHWLSeJXX6i4nSLPr1C1DNmiLkY130_provenance
{
dgn-np:NP262896.RAod_mIpvuX0CTa55mEHWLSeJXX6i4nSLPr1C1DNmiLkY130_assertion
dcterms:description
"[The genes NEUROG2, ANK2, UGT8 and CAMK2D, which are known to be expressed in human brain, are strong positional candidates and we propose to examine these and other genes in the locus to identify the causative gene for this intriguing form of epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:19597845
;
prov:wasDerivedFrom
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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:NP262896.RAod_mIpvuX0CTa55mEHWLSeJXX6i4nSLPr1C1DNmiLkY130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
dgn-void:disgenetrdf
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> , <
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> , <
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> ;
pav:createdBy
<
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