@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc
> .
@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:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_head
{
this:
np:hasAssertion
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_assertion
;
np:hasProvenance
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_provenance
;
np:hasPublicationInfo
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_assertion
a
np:Assertion
.
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_provenance
a
np:Provenance
.
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_assertion
{
miriam-gene:5698
a
ncit:C16612
.
lld:C0038013
a
ncit:C7057
.
dgn-gda:DGN4261d2b2d33af25fde4fdd87e1aeef4d
sio:SIO_000628
miriam-gene:5698
,
lld:C0038013
;
a
sio:SIO_001121
.
}
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_provenance
{
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_assertion
dcterms:description
"[A polymorphic CfoI restriction enzyme site in the coding region of the LMP2 gene was evaluated in genomic DNA samples from 193 white and 49 Chinese B27 individuals with well documented AS, 97 of whom had had acute anterior uveitis (AAU) and 97 peripheral arthritis; 42 samples from normal, white, B27 positive blood donors in whom AS was excluded were also evaluated.]. 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:7763114
;
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:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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" .
}