@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI
> .
@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:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_head
{
this:
np:hasAssertion
dgn-np:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_assertion
;
np:hasProvenance
dgn-np:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_provenance
;
np:hasPublicationInfo
dgn-np:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_assertion
a
np:Assertion
.
dgn-np:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_provenance
a
np:Provenance
.
dgn-np:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_assertion
{
miriam-gene:10724
a
ncit:C16612
.
lld:C0032339
a
ncit:C7057
.
dgn-gda:DGN707a787783a81eb4ee274cf5d21e0698
sio:SIO_000628
miriam-gene:10724
,
lld:C0032339
;
a
sio:SIO_001121
.
}
dgn-np:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_provenance
{
dgn-np:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_assertion
dcterms:description
"[These findings therefore underscore the functional importance of the PHD finger in vivo and imply that reduction of CBP HAT activity, as exemplified here by disruption of the PHD finger, is sufficient to cause RTS.]. 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:12566391
;
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:NP927864.RAxsEMPBRUaOMaml1paTSeDgLWumP_jygghXTYMjrdgxI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:29+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" .
}