@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo
> .
@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:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_head
{
this:
np:hasAssertion
dgn-np:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_assertion
;
np:hasProvenance
dgn-np:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_provenance
;
np:hasPublicationInfo
dgn-np:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_assertion
a
np:Assertion
.
dgn-np:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_provenance
a
np:Provenance
.
dgn-np:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_assertion
{
miriam-gene:821
a
ncit:C16612
.
lld:C0259810
a
ncit:C7057
.
dgn-gda:DGN1922243a9053e40e410090ebf0a383f6
sio:SIO_000628
miriam-gene:821
,
lld:C0259810
;
a
sio:SIO_001121
.
}
dgn-np:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_provenance
{
dgn-np:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_assertion
dcterms:description
"[These results show that functional dRTA mutants are retained in the ER due to their interaction with molecular chaperones, particularly calnexin, and that disruption of these interactions can promote their escape from the ER and cell surface rescue.]. 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:20628050
;
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:NP160922.RAyutIDy3kDB9RE7sV4sHrlPthdkd2mKY4J0aAK_vUKKo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}