@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw
> .
@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:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_head
{
this:
np:hasAssertion
dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_assertion
;
np:hasProvenance
dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_provenance
;
np:hasPublicationInfo
dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_assertion
a
np:Assertion
.
dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_provenance
a
np:Provenance
.
dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_assertion
{
miriam-gene:100188848
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN1672121d5b6b2d095edeeb1c3c403d76
sio:SIO_000628
miriam-gene:100188848
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_provenance
{
dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_assertion
dcterms:description
"[Interestingly, mossy fiber sprouting was less pronounced in patients with FMTLE, suggesting that, when compared to SMTLE, patients with FMTLE respond differently to plastic changes plausibly induced by cell loss, neuronal deafferentation, or epileptic seizures.]. 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:18294201
;
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:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:15+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" .
}