@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw
> .
@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:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_head
{
this:
np:hasAssertion
dgn-np:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_assertion
;
np:hasProvenance
dgn-np:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_provenance
;
np:hasPublicationInfo
dgn-np:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_assertion
a
np:Assertion
.
dgn-np:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_provenance
a
np:Provenance
.
dgn-np:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_assertion
{
miriam-gene:581
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN88720e13b163897077f738e2d1d53fc3
sio:SIO_000628
miriam-gene:581
,
lld:C0026769
;
a
sio:SIO_001122
.
}
dgn-np:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_provenance
{
dgn-np:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_assertion
dcterms: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:NP47889.RAWfDgFr2p5hAbs3A1AN4nvC0EevkGEL5JNg5neNdTaHw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}