@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo
> .
@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:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_head
{
this:
np:hasAssertion
dgn-np:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_assertion
;
np:hasProvenance
dgn-np:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_provenance
;
np:hasPublicationInfo
dgn-np:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_assertion
a
np:Assertion
.
dgn-np:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_provenance
a
np:Provenance
.
dgn-np:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_assertion
{
miriam-gene:4864
a
ncit:C16612
.
lld:C0231341
a
ncit:C7057
.
dgn-gda:DGNfec73a79c5d01f907b0f1719f0d2c5a7
sio:SIO_000628
miriam-gene:4864
,
lld:C0231341
;
a
sio:SIO_001121
.
}
dgn-np:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_provenance
{
dgn-np:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_assertion
dcterms:description
"[Two mutants, causing prenatal skin disease restrictive dermopathy (RD) and the premature aging disease Hutchinson Gilford progeria syndrome, were used for expression in HeLa cells to investigate their impact on the subcellular localization of NPC-associated proteins and nuclear protein import.]. 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:19442658
;
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:NP539341.RALqkH_ANQfWTk2gWaBU5ttcAO0n3la1guo7jVyf1w3wo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}