@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54
> .
@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:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_head
{
this:
np:hasAssertion
dgn-np:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_assertion
;
np:hasProvenance
dgn-np:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_provenance
;
np:hasPublicationInfo
dgn-np:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_assertion
a
np:Assertion
.
dgn-np:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_provenance
a
np:Provenance
.
dgn-np:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_assertion
{
miriam-gene:1234
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGNf870ab7540c2069efee558fec2d30252
sio:SIO_000628
miriam-gene:1234
,
lld:C0026769
;
a
sio:SIO_001122
.
}
dgn-np:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_provenance
{
dgn-np:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_assertion
dct:description
"[These results represent an independent validation of MS association with DRB1*15(2) and TNFa9 in Russians and are the first to find the interplay of three loci in conferring susceptibility to MS. They demonstrate the efficacy of our approach for the identification of complex-disease-associated combinations of alleles.]. 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:16872485
;
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:NP47256.RAuT2YIhDQdhjZE9l6yGVhrJaRBdlbK59M-40N1QM4K54130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+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" .
}