@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses
> .
@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:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_head
{
this:
np:hasAssertion
dgn-np:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_assertion
;
np:hasProvenance
dgn-np:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_provenance
;
np:hasPublicationInfo
dgn-np:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_assertion
a
np:Assertion
.
dgn-np:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_provenance
a
np:Provenance
.
dgn-np:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_assertion
{
miriam-gene:266629
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNedac5d207dba14e8715d6bba500bc36b
sio:SIO_000628
miriam-gene:266629
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_provenance
{
dgn-np:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_assertion
dcterms:description
"[Despite possible sampling error, the lack of a difference in TAP2 status between cases and controls within ethnic groups and, if anything, an inverse association across ethnic groups, makes it unlikely that the TAP2 polymorphism studied here is of primary relevance to SLE susceptibility.]. 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:8670572
;
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:NP933162.RAz3jUCxdcGDOmHz7h6N5yipwjHvACg-VG58vab66wses130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:32+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" .
}