@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU
> .
@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:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_head
{
this:
np:hasAssertion
dgn-np:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_assertion
;
np:hasProvenance
dgn-np:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_provenance
;
np:hasPublicationInfo
dgn-np:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_assertion
a
np:Assertion
.
dgn-np:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_provenance
a
np:Provenance
.
dgn-np:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_assertion
{
miriam-gene:7415
a
ncit:C16612
.
lld:C1283761
a
ncit:C7057
.
dgn-gda:DGNb5a50b22a97741704f84f4d20f9ba0ef
sio:SIO_000628
miriam-gene:7415
,
lld:C1283761
;
a
sio:SIO_001121
.
}
dgn-np:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_provenance
{
dgn-np:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_assertion
dcterms:description
"[We predict that selective interference of VCP interaction(s) with aberrant protein or its ERAD function will be an effective therapeutic site to rescue functional misfolded protein in diseases like cystic fibrosis and alpha-1-trypsin deficiency.]. 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:18798739
;
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:NP753872.RAAomIhP56lJr1xcHFG3IUfrEEDCS7noUKkSQpYMemzdU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}