@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o
> .
@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:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_head
{
this:
np:hasAssertion
dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_assertion
;
np:hasProvenance
dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_provenance
;
np:hasPublicationInfo
dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_assertion
a
np:Assertion
.
dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_provenance
a
np:Provenance
.
dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_assertion
{
miriam-gene:199699
a
ncit:C16612
.
lld:C0271994
a
ncit:C7057
.
dgn-gda:DGNe6e7bf953d9edb4df4ec09d358a35a12
sio:SIO_000628
miriam-gene:199699
,
lld:C0271994
;
a
sio:SIO_001121
.
}
dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_provenance
{
dgn-np:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_assertion
dcterms:description
"[Gel mobility shift assays with nuclear extract from K562 cells (which contain both Sp1 and SSP) demonstrate preferential binding of SSP to the SSE and HPFH sites under conditions in which probe was limiting.]. 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:7684493
;
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:NP693192.RAxSBEZaMdio-6CCdmslufgxmqoJs8fD_1uM0-M8ME86o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:01+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" .
}