@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M
> .
@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/v4.0.0/void/
> .
dgn-np:NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M130_head
{
this:
np:hasAssertion
dgn-np:NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M130_assertion
a
np:Assertion
.
dgn-np:NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M130_provenance
a
np:Provenance
.
dgn-np:NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M130_assertion
{
miriam-gene:817
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN4d7622503890a5377cd0d43198250e55
sio:SIO_000628
miriam-gene:817
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M130_provenance
{
dgn-np:NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M130_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
;
sio:SIO_000772
miriam-pubmed:19597845
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP751097.RAFeM_xEnLDW22QGdeQCFirFMYUPTPj6Bt_e0LUCuOp1M130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:25+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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}