@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE130_assertion
;
np:hasProvenance
dgn-np:NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE130_provenance
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np:hasPublicationInfo
dgn-np:NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE130_assertion
a
np:Assertion
.
dgn-np:NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE130_provenance
a
np:Provenance
.
dgn-np:NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE130_assertion
{
miriam-gene:3407
a
ncit:C16612
.
lld:C0004364
a
ncit:C7057
.
dgn-gda:DGN53c65ddda2b174d6b60f306336c751df
sio:SIO_000628
miriam-gene:3407
,
lld:C0004364
;
a
sio:SIO_001121
.
}
dgn-np:NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE130_provenance
{
dgn-np:NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE130_assertion
dcterms:description
"[The aim of this study was to fine map the IDDM8 region on chromosome 6q27, focusing on the genes in the region, to identify polymorphisms that may contribute to susceptibility to RA and potentially to other autoimmune diseases.]. 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:16945141
;
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:NP858639.RAc4rWrnkDRTV50Y1Rw86-xCjZdcJV3gbS9Z9y4-ChXXE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:45+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" .
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pav:version
"v2.1.0" .
}