@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY
> .
@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:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_head
{
this:
np:hasAssertion
dgn-np:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_assertion
;
np:hasProvenance
dgn-np:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_provenance
;
np:hasPublicationInfo
dgn-np:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_assertion
a
np:Assertion
.
dgn-np:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_provenance
a
np:Provenance
.
dgn-np:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_assertion
{
miriam-gene:6304
a
ncit:C16612
.
lld:C0848332
a
ncit:C7057
.
dgn-gda:DGNdf96edcaf23d297bafb669a3f5871417
sio:SIO_000628
miriam-gene:6304
,
lld:C0848332
;
a
sio:SIO_001121
.
}
dgn-np:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_provenance
{
dgn-np:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_assertion
dcterms:description
"[In vivo SATB1-binding sequences hybridized to genomic DNA as single spots within the residual nucleus circumscribed by the halo of DNA and remained as single spots in the nuclear matrix, indicating that these sequences are localized at the base of chromatin loops.]. 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:9548713
;
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:NP379310.RAFIl1Lfe97GwYz_OcyU2tscuWYlKa2l9kU2L1BoDtIsY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:44+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" .
}