@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA
> .
@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:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_head
{
this:
np:hasAssertion
dgn-np:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_assertion
;
np:hasProvenance
dgn-np:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_provenance
;
np:hasPublicationInfo
dgn-np:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_assertion
a
np:Assertion
.
dgn-np:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_provenance
a
np:Provenance
.
dgn-np:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_assertion
{
miriam-gene:11277
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNe16a8b7648a7ab9f3378fa87963937dc
sio:SIO_000628
miriam-gene:11277
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_provenance
{
dgn-np:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_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:NP244359.RA57lEBj9_rk6v3LahCLYN3MjkmmngXNuDL39Zm1zM5LA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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" .
}