@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY
> .
@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:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_head
{
this:
np:hasAssertion
dgn-np:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_assertion
;
np:hasProvenance
dgn-np:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_provenance
;
np:hasPublicationInfo
dgn-np:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_assertion
a
np:Assertion
.
dgn-np:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_provenance
a
np:Provenance
.
dgn-np:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_assertion
{
miriam-gene:3117
a
ncit:C16612
.
lld:C0003864
a
ncit:C7057
.
dgn-gda:DGN51aa9de4f25ab40d9099e3354e513de4
sio:SIO_000628
miriam-gene:3117
,
lld:C0003864
;
a
sio:SIO_001122
.
}
dgn-np:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_provenance
{
dgn-np:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_assertion
dcterms:description
"[ The DQ3-DR4/9 haplotypes are associated with RA. The DQ5-DR1/10 haplotypes are associated with less active disease, i.e. UA, and DERAA encoding DRB1 alleles modulate either predisposition to or the severity of RA. We propose that HLA polymorphism influences not only the initiation or perpetuation of RA but also protection against the disease.]. 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:11257148
;
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:NP58046.RALLtajSHwLtYBDJKIaEwgtdWWfeLXfDqa7JZraOssUwY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}