@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U
> .
@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:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_head
{
this:
np:hasAssertion
dgn-np:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_assertion
;
np:hasProvenance
dgn-np:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_provenance
;
np:hasPublicationInfo
dgn-np:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_assertion
a
np:Assertion
.
dgn-np:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_provenance
a
np:Provenance
.
dgn-np:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_assertion
{
miriam-gene:246319
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN92ae35c7665713434ba0f90412d6ca34
sio:SIO_000628
miriam-gene:246319
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_provenance
{
dgn-np:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_assertion
dcterms:description
"[In Vogt-Koyanagi-Harada disease, inflammatory disorders occur in multiple organs containing melanocytes, including uvea (resulting in acute bilateral panuveitis), skin (resulting in vitiligo and alopecia), central nervous system (resulting in meningitis) and inner ears (resulting in hearing loss and tinnitus).]. 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:11578690
;
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:NP597089.RAPmfke-aljkjBHOqO3WKZDy8uipWhGLQcympvgD_nW1U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}