@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ
> .
@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:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_head
{
this:
np:hasAssertion
dgn-np:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_assertion
;
np:hasProvenance
dgn-np:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_assertion
a
np:Assertion
.
dgn-np:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_provenance
a
np:Provenance
.
dgn-np:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_assertion
{
miriam-gene:129831
a
ncit:C16612
.
lld:C2347126
a
ncit:C7057
.
dgn-gda:DGNdbc64b38317f2c8b7ee5f8277bb5cd35
sio:SIO_000628
miriam-gene:129831
,
lld:C2347126
;
a
sio:SIO_001121
.
}
dgn-np:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_provenance
{
dgn-np:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_assertion
dcterms:description
"[These results indicate that DRB1*0901-DQB1*0303 haplotype represents the primary genetic risk for MPA within the HLA region in Japanese, and provides the basis that future functional studies on the role of HLA in MPA should target DR9, DQ9 and DR53 proteins encoded by this haplotype.]. 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:16208405
;
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:NP327518.RAdwmGuOfaUl80dr_u9BGJFdRjqxLTpnmDzkUyMgMGTbQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:11+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" .
}