@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM
> .
@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:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_head
{
this:
np:hasAssertion
dgn-np:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_assertion
;
np:hasProvenance
dgn-np:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_provenance
;
np:hasPublicationInfo
dgn-np:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_assertion
a
np:Assertion
.
dgn-np:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_provenance
a
np:Provenance
.
dgn-np:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_assertion
{
miriam-gene:100188848
a
ncit:C16612
.
lld:C0014556
a
ncit:C7057
.
dgn-gda:DGN1ed70c5d120dc02348586f00b1f3fbe3
sio:SIO_000628
miriam-gene:100188848
,
lld:C0014556
;
a
sio:SIO_001121
.
}
dgn-np:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_provenance
{
dgn-np:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_assertion
dcterms:description
"[The genetics of these conditions is largely unknown and the hope for the future is that the identification of FMTLE genes will lead to more appropriate approaches for the diagnosis and treatment of TLE.]. 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:19469849
;
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:NP179246.RAK1saQg8L64uYYyogvJXYRZhXFW2bJwzHTz6s5T9Z-IM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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" .
}