@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw
> .
@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:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_head
{
this:
np:hasAssertion
dgn-np:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_assertion
;
np:hasProvenance
dgn-np:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_provenance
;
np:hasPublicationInfo
dgn-np:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_assertion
a
np:Assertion
.
dgn-np:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_provenance
a
np:Provenance
.
dgn-np:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_assertion
{
miriam-gene:1523
a
ncit:C16612
.
lld:C1868112
a
ncit:C7057
.
dgn-gda:DGN483f387d227e6a88c79480eae14cd209
sio:SIO_000628
miriam-gene:1523
,
lld:C1868112
;
a
sio:SIO_001121
.
}
dgn-np:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_provenance
{
dgn-np:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_assertion
dcterms:description
"[Here we report that a 13 nucleotides deletion in the CCAAT box region of the A gamma-globin promoter, associated with greater than 100 fold overexpression of the gene, abolishes the in vitro binding of the ubiquitous factors CP1 and CDP (CCAAT displacement protein) and of the erythroid specific protein NFE3.]. 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:2476717
;
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:NP688405.RAkYgMimJfmSXolNvqffbKUH9_Tj7-MkPqysvDdN2d-Xw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}