@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4
> .
@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:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_head
{
this:
np:hasAssertion
dgn-np:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_assertion
;
np:hasProvenance
dgn-np:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_provenance
;
np:hasPublicationInfo
dgn-np:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_assertion
a
np:Assertion
.
dgn-np:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_provenance
a
np:Provenance
.
dgn-np:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_assertion
{
miriam-gene:6646
a
ncit:C16612
.
lld:C0268164
a
ncit:C7057
.
dgn-gda:DGN187dd1377f5e61b904f1220f48a5017f
sio:SIO_000628
miriam-gene:6646
,
lld:C0268164
;
a
sio:SIO_001121
.
}
dgn-np:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_provenance
{
dgn-np:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_assertion
dcterms:description
"[We have further shown that the unphosphorylated or 'transcriptionally inactive' form of STAT92E is localized on heterochromatin in association with HP1, and is required for stabilizing HP1 localization and histone H3 Lys 9 methylation (H3mK9) .]. 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:18344984
;
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:NP925755.RA2GE3FuW-oZ81cuvTqLtEPQa-hx9e_VghqTrrb2KoWI4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}