@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM
> .
@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:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_head
{
this:
np:hasAssertion
dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_assertion
;
np:hasProvenance
dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_provenance
;
np:hasPublicationInfo
dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_assertion
a
np:Assertion
.
dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_provenance
a
np:Provenance
.
dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_assertion
{
miriam-gene:2571
a
ncit:C16612
.
lld:C0600327
a
ncit:C7057
.
dgn-gda:DGNf793fae67b411e8575d37bb38d7fc4e7
sio:SIO_000628
miriam-gene:2571
,
lld:C0600327
;
a
sio:SIO_001121
.
}
dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_provenance
{
dgn-np:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_assertion
dcterms:description
"[The GAD1-TSS(-50kbLoop) was enriched with nucleosomes epigenetically decorated with the transcriptional mark, histone H3 trimethylated at lysine 4, and was weak or absent in skin fibroblasts and pluripotent stem cells compared with neuronal cultures differentiated from them.]. 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:23864674
;
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:NP574288.RArNXION7boonK8SVfbBDZMY1vVpXj7s40MHucN9j65mM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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" .
}