@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c
> .
@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:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_head
{
this:
np:hasAssertion
dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_assertion
;
np:hasProvenance
dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_provenance
;
np:hasPublicationInfo
dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_assertion
a
np:Assertion
.
dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_provenance
a
np:Provenance
.
dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_assertion
{
miriam-gene:80381
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN655c75304d878585e51b6373080d3e57
sio:SIO_000628
miriam-gene:80381
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_provenance
{
dgn-np:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_assertion
dcterms:description
"[A whole genome association scan suggested that allelic variants in the CD58 gene region, encoding the costimulatory molecule LFA-3, are associated with risk of developing MS. We now report additional genetic evidence, as well as resequencing and fine mapping of the CD58 locus in patients with MS and control subjects.]. 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:19237575
;
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:NP739691.RAiaStM0urgzzw7SlD2_hD7igYfvgMTJz8FBq1ZKqp-4c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+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" .
}