@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8
> .
@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:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_head
{
this:
np:hasAssertion
dgn-np:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_assertion
;
np:hasProvenance
dgn-np:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_provenance
;
np:hasPublicationInfo
dgn-np:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_assertion
a
np:Assertion
.
dgn-np:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_provenance
a
np:Provenance
.
dgn-np:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0151449
a
ncit:C7057
.
dgn-gda:DGN8dab8cdafc39ac363e211f5621699a2a
sio:SIO_000628
miriam-gene:6520
,
lld:C0151449
;
a
sio:SIO_001121
.
}
dgn-np:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_provenance
{
dgn-np:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_assertion
dcterms:description
"[The relationships of human leukocyte antigen (HLA) and heavy chain immunoglobulin (Gm) haplotypes to disease and autoantibody expression were examined in six large kindreds, each having one or more members with primary Sjögren's syndrome.]. 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:6437309
;
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:NP280405.RAB6KU5jA2Z15QSzX5IFRID-wlRNn__17NUjVk0arR8N8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}