@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_head
{
this:
np:hasAssertion
dgn-np:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_assertion
;
np:hasProvenance
dgn-np:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_provenance
;
np:hasPublicationInfo
dgn-np:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_assertion
a
np:Assertion
.
dgn-np:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_provenance
a
np:Provenance
.
dgn-np:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGN1b7965c419df903cb8b69ec8656804e4
sio:SIO_000628
miriam-gene:4204
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_provenance
{
dgn-np:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_assertion
dcterms:description
"[Using neuronal progenitor cells derived from human induced pluripotent stem cells and human tissues, we revealed that patients with Rett syndrome (RTT), carrying MeCP2 mutations, have increased susceptibility for L1 retrotransposition.]. 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:21085180
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP853124.RAbmqOv7LMgguCo1_mmjdjWqkUWoX4ZViHQ6j0QEPgDMk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:11+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}