@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk
> .
@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:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_head
{
this:
np:hasAssertion
dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_assertion
;
np:hasProvenance
dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_provenance
;
np:hasPublicationInfo
dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_assertion
a
np:Assertion
.
dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_provenance
a
np:Provenance
.
dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_assertion
{
miriam-gene:5698
a
ncit:C16612
.
lld:C0003864
a
ncit:C7057
.
dgn-gda:DGN3785d91e0641dd03fd7f3b82938792d5
sio:SIO_000628
miriam-gene:5698
,
lld:C0003864
;
a
sio:SIO_001121
.
}
dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_provenance
{
dgn-np:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_assertion
dcterms:description
"[Our data is thus internally consistent in demonstrating no association between LMP2 genotypes and either disease severity or peripheral arthritis, and supports the notion that polymorphism of LMP2 primarily influences the development of AAU and not some other phenotype of AS.]. 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:9348140
;
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:NP581103.RA3FSkR739VTuU3TtFdqYDdWMDSCTsgQJQtNeO54Yzmlk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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" .
}