@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU
> .
@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:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_head
{
this:
np:hasAssertion
dgn-np:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_assertion
;
np:hasProvenance
dgn-np:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_provenance
;
np:hasPublicationInfo
dgn-np:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_assertion
a
np:Assertion
.
dgn-np:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_provenance
a
np:Provenance
.
dgn-np:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_assertion
{
miriam-gene:29980
a
ncit:C16612
.
lld:C0949691
a
ncit:C7057
.
dgn-gda:DGNca35b2478cb9757cd20a556005c92ab3
sio:SIO_000628
miriam-gene:29980
,
lld:C0949691
;
a
sio:SIO_001121
.
}
dgn-np:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_provenance
{
dgn-np:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_assertion
dcterms:description
"[When these new findings are added to the previous observations that acute anterior uveitis probably is a clinical, sex-influenced characteristic of HLA B27 positive Bechterew's syndrome, that HLA B27 negative patients with Bechterew's syndrome frequently had psoriasis and were HLA B13 and B17 negative, and that psoriasis was frequent in HLA B27 positive patients as well, we tentatively conclude that different and interacting genetic mechanisms may be involved in the etiology of Bechterew'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:6983935
;
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:NP545702.RAwcXAfnv4c3Pv1KZ6RdiWXIjm0waHjNK0N4n2HtVT2CU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:29+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" .
}