@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw
> .
@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:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_head
{
this:
np:hasAssertion
dgn-np:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_assertion
;
np:hasProvenance
dgn-np:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_provenance
;
np:hasPublicationInfo
dgn-np:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_assertion
a
np:Assertion
.
dgn-np:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_provenance
a
np:Provenance
.
dgn-np:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_assertion
{
miriam-gene:9211
a
ncit:C16612
.
lld:C0234461
a
ncit:C7057
.
dgn-gda:DGNfd60cc3d16755ec00df2d3c0dffaaff4
sio:SIO_000628
miriam-gene:9211
,
lld:C0234461
;
a
sio:SIO_001121
.
}
dgn-np:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_provenance
{
dgn-np:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_assertion
dcterms:description
"[Our data confirm the inclusion of aphasic seizures within the ADLTE clinical spectrum, suggest the existence of locus heterogeneity in ADLTE, and provide new familial cases with LGI1 missense mutations associated with the disease.]. 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:14510822
;
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:NP852563.RA9SGDzaU853P4I2lIL9Im7_nQUatwsFnv8cp7SRHBadw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:41+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" .
}