@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw
> .
@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:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_head
{
this:
np:hasAssertion
dgn-np:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_assertion
;
np:hasProvenance
dgn-np:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_provenance
;
np:hasPublicationInfo
dgn-np:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_assertion
a
np:Assertion
.
dgn-np:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_provenance
a
np:Provenance
.
dgn-np:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_assertion
{
miriam-gene:9734
a
ncit:C16612
.
lld:C0013264
a
ncit:C7057
.
dgn-gda:DGNf68d60753b3600a8a3dada8cfb2ccd25
sio:SIO_000628
miriam-gene:9734
,
lld:C0013264
;
a
sio:SIO_001121
.
}
dgn-np:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_provenance
{
dgn-np:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_assertion
dcterms:description
"[Studies performed in mouse models of Duchenne muscular dystrophy (DMD) indicate that dystrophin deficiency leads to deregulated HDAC activity, which perturbs downstream networks and can be restored directly, by HDAC blockade, or indirectly, by reexpression of dystrophin.]. 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:21308150
;
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:NP562064.RAbB2fUoU89Gkwxggb7_Uyla-tVYOPL1GFbatND5z0Ssw130_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" .
}