@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0
> .
@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 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:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_head
{
this:
np:hasAssertion
dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_assertion
;
np:hasProvenance
dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_provenance
;
np:hasPublicationInfo
dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_assertion
a
np:Assertion
.
dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_provenance
a
np:Provenance
.
dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_assertion
{
miriam-gene:596
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN696e8a499c346fc42e3f57e136aa661a
sio:SIO_000628
miriam-gene:596
,
lld:C0026769
;
a
sio:SIO_001122
.
}
dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_provenance
{
dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_assertion
dct:description
"[No significant differences in the frequency of gene sequence variations were found between MS patients and controls. The apoptosis genes studied here therefore appear less likely to be important effector genes in MS.]. 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:12161031
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}