@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs130_assertion
;
np:hasProvenance
dgn-np:NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs130_provenance
;
np:hasPublicationInfo
dgn-np:NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs130_assertion
a
np:Assertion
.
dgn-np:NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs130_provenance
a
np:Provenance
.
dgn-np:NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs130_assertion
{
miriam-gene:6792
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGNee9da59a8132dff8cb6c199b908cfabd
sio:SIO_000628
miriam-gene:6792
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs130_provenance
{
dgn-np:NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs130_assertion
dcterms:description
"[Because CDKL5, which is involved in the early-onset variant of Rett syndrome, is also located in these speckles, we suggest that disregulation of the dynamic behaviour of nuclear speckles may functionally link these two proteins, which are both involved in atypical forms of Rett syndrome.]. 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:21280142
;
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:NP200550.RAm_EkCe0sStY6YiuHnn053piTQ16_-L_VQjLTZayVaYs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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
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"v2.1.0" .
}