@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg
> .
@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:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_head
{
this:
np:hasAssertion
dgn-np:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_assertion
;
np:hasProvenance
dgn-np:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_provenance
;
np:hasPublicationInfo
dgn-np:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_assertion
a
np:Assertion
.
dgn-np:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_provenance
a
np:Provenance
.
dgn-np:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_assertion
{
miriam-gene:1385
a
ncit:C16612
.
lld:C0032339
a
ncit:C7057
.
dgn-gda:DGNafb391020dc57602addcf0553afd4e70
sio:SIO_000628
miriam-gene:1385
,
lld:C0032339
;
a
sio:SIO_001121
.
}
dgn-np:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_provenance
{
dgn-np:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_assertion
dcterms:description
"[These findings suggest that some of the cognitive and physiological deficits observed on RTS are not simply due to the reduction of CBP during development but may also result from the continued requirement throughout life for both the CREB co-activation and the histone acetylation function of CBP.]. 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:15207239
;
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:NP910574.RA_l9hdyrcsVuSI9D9hGSncuCpmYOfyunwnVMFnfacYbg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}