@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q
> .
@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:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_head
{
this:
np:hasAssertion
dgn-np:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_assertion
;
np:hasProvenance
dgn-np:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_assertion
a
np:Assertion
.
dgn-np:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_provenance
a
np:Provenance
.
dgn-np:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C2675212
a
ncit:C7057
.
dgn-gda:DGNcff05938bf6dea4cedeb0c06534f23bf
sio:SIO_000628
miriam-gene:6520
,
lld:C2675212
;
a
sio:SIO_001121
.
}
dgn-np:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_provenance
{
dgn-np:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_assertion
dcterms:description
"[Nuclear factor kappaB binding sites were shown to be primarily responsible for the positive activity contributed by the HS1,2 and HS4 regions, and we observed the in vivo interaction of these factors with the human immunoglobulin heavy chain gene enhancer regions in t(14;18) cells.]. 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:14583460
;
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:NP794170.RAyQCqZDT4sVzljC2X-YPPhweoBNarN5mWE4E8BJRQW-Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+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" .
}