@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ
> .
@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:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_head
{
this:
np:hasAssertion
dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_assertion
;
np:hasProvenance
dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_assertion
a
np:Assertion
.
dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_provenance
a
np:Provenance
.
dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_assertion
{
miriam-gene:8718
a
ncit:C16612
.
lld:C0021053
a
ncit:C7057
.
dgn-gda:DGN853b39183b1e10d8232ac803fce7f68c
sio:SIO_000628
miriam-gene:8718
,
lld:C0021053
;
a
sio:SIO_001121
.
}
dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_provenance
{
dgn-np:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_assertion
dcterms:description
"[Based on these findings and those in other autoimmune diseases it is considered that the haplotype Bw46, DRw9 in Chinese takes the place of B8, DR3 in Caucasians in carrying genes which predispose to the development of auto-immune 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:3472422
;
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:NP573017.RAVSVZftaO9JCYM8lsl56TQe5dMqgXQ6pCDwmMkxRn4aQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}