@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo
> .
@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:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_head
{
this:
np:hasAssertion
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_assertion
;
np:hasProvenance
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_assertion
a
np:Assertion
.
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_provenance
a
np:Provenance
.
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGN76a1b2e2d77cc609ec2be0da887135ec
sio:SIO_000628
miriam-gene:4204
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_provenance
{
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_assertion
dcterms:description
"[Reversal of phenotypes in adult symptomatic mice has been demonstrated in some models of monogenic loss-of-function neurological disorders, including loss of MeCP2 in Rett syndrome, indicating that, at least in some cases, the neuroanatomy may remain sufficiently intact so that correction of the molecular dysfunction underlying these disorders can restore healthy physiology.]. 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:26605526
;
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:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:33+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" .
}