@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk
> .
@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:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_head
{
this:
np:hasAssertion
dgn-np:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_assertion
;
np:hasProvenance
dgn-np:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_provenance
;
np:hasPublicationInfo
dgn-np:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_assertion
a
np:Assertion
.
dgn-np:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_provenance
a
np:Provenance
.
dgn-np:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_assertion
{
miriam-gene:11277
a
ncit:C16612
.
lld:C0024145
a
ncit:C7057
.
dgn-gda:DGN2c46ea6134cbf06adbf68e6ecde11f1a
sio:SIO_000628
miriam-gene:11277
,
lld:C0024145
;
a
sio:SIO_001121
.
}
dgn-np:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_provenance
{
dgn-np:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_assertion
dcterms:description
"[Other groups have shown that the syndromes of familial chilblain lupus as well as systemic lupus erythematosus, and the distinct neurovascular disorder retinal vasculopathy with cerebral leukodystrophy, can be caused by dominant mutations at different sites within the TREX1 gene.]. 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:19442247
;
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:NP620382.RAjE25Dy7IHKpjhz-MCq5irRBohlCS5Ig1BGGa_dehsPk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:14+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" .
}