@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE
> .
@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:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_head
{
this:
np:hasAssertion
dgn-np:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_assertion
;
np:hasProvenance
dgn-np:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_provenance
;
np:hasPublicationInfo
dgn-np:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_assertion
a
np:Assertion
.
dgn-np:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_provenance
a
np:Provenance
.
dgn-np:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_assertion
{
miriam-gene:1410
a
ncit:C16612
.
lld:C1839780
a
ncit:C7057
.
dgn-gda:DGNa0944abf8705c979f8ffdaa467eac9a4
sio:SIO_000628
miriam-gene:1410
,
lld:C1839780
;
a
sio:SIO_001121
.
}
dgn-np:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_provenance
{
dgn-np:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_assertion
dcterms:description
"[Here we report a cellular endophenotype involving increased stress response (HSP27, HSP70 and CRYAB) and altered lamin A/C expression/organization in cultured skin fibroblasts from 11 male carriers of premutation alleles of the FMR1 gene, including six patients with FXTAS and five premutation carriers with no clinical evidence of FXTAS, compared with six controls.]. 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:19864489
;
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:NP347214.RAQAf97LoQvIvEdVbaWDNP-QV-WHsC0uSlVyAWqatNpXE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:24+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" .
}