@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM
> .
@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:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_head
{
this:
np:hasAssertion
dgn-np:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_assertion
;
np:hasProvenance
dgn-np:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_provenance
;
np:hasPublicationInfo
dgn-np:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_assertion
a
np:Assertion
.
dgn-np:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_provenance
a
np:Provenance
.
dgn-np:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_assertion
{
miriam-gene:5696
a
ncit:C16612
.
lld:C0036202
a
ncit:C7057
.
dgn-gda:DGNed1187ad5a8340c53d66716f8f93a638
sio:SIO_000628
miriam-gene:5696
,
lld:C0036202
;
a
sio:SIO_001121
.
}
dgn-np:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_provenance
{
dgn-np:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_assertion
dcterms:description
"[No differences were found between either of the patient groups and the healthy control group, indicating that LMP7 allelic variation may not contribute to the pathogenesis of either Behçet's disease or sarcoidosis.]. 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:8960913
;
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:NP679168.RA3deGVTcXJ3dAX6VvXLQ80UHLp9UXcN-hDc3-Pek6CrM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:50+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" .
}