@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k
> .
@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:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_head
{
this:
np:hasAssertion
dgn-np:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_assertion
;
np:hasProvenance
dgn-np:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_provenance
;
np:hasPublicationInfo
dgn-np:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_assertion
a
np:Assertion
.
dgn-np:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_provenance
a
np:Provenance
.
dgn-np:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_assertion
{
miriam-gene:55638
a
ncit:C16612
.
lld:C0041341
a
ncit:C7057
.
dgn-gda:DGN76f05001bf9c610f2da1066ac76da8b3
sio:SIO_000628
miriam-gene:55638
,
lld:C0041341
;
a
sio:SIO_001121
.
}
dgn-np:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_provenance
{
dgn-np:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_assertion
dcterms:description
"[The prominent postnatal expression of DCL by BCs/GCs and DNs in FCD and TSC supports an important role for this microtubule associated protein, also during early human cortical development, which could be relevant to the pathogenesis of these developmental glioneuronal malformations.]. 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:19583781
;
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:NP562967.RAnEXfP3y4xUrp6AhObbEfVNWUP9VORHM9kkVTvKgnW9k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}